Clinical characteristics.

Huntington disease (HD) is a progressive disorder of motor, cognitive, and psychiatric disturbances. The mean age of onset is 35 to 44 years, and the median survival time is 15 to 18 years after onset.

Diagnosis/testing.

The diagnosis of HD rests on positive family history, characteristic clinical findings, and the detection of an expansion of 36 or more CAG trinucleotide repeats in HTT.

Management.

Treatment of manifestations: Pharmacologic therapy including typical neuroleptics (haloperidol), atypical neuroleptics (olanzapine), benzodiazepines, or the monoamine-depleting agent tetrabenazine for choreic movements; anti-parkinsonian agents for hypokinesia and rigidity; psychotropic drugs or some types of anti-seizure medication for psychiatric disturbances (depression, psychotic symptoms, outbursts of aggression); valproic acid for myoclonic hyperkinesia. Supportive care with attention to nursing needs, dietary intake, special equipment, and eligibility for state and federal benefits.

Prevention of secondary complications: Attention to the usual potential complications in persons requiring long-term supportive care and to side effects associated with pharmacologic treatments.

Surveillance: Regular evaluations of the appearance and severity of chorea, rigidity, gait abnormalities, depression, behavioral changes, and cognitive decline; routine assessment of functional abilities using the Behavior Observation Scale Huntington (BOSH) and the Unified Huntington's Disease Rating Scale (UHDRS).

Agents/circumstances to avoid: L-dopa-containing compounds (may increase chorea), alcohol consumption, smoking.

Other: Children and adolescents with a parent with HD may benefit from referral to a local HD support group for educational materials and psychological support.

Genetic counseling.

HD is inherited in an autosomal dominant manner. Offspring of an individual with a pathogenic variant have a 50% chance of inheriting the disease-causing allele. Predictive testing in asymptomatic adults at risk is available but requires careful thought (including pre- and post-test genetic counseling) as there is currently no cure for the disorder. However, asymptomatic individuals at risk may be eligible to participate in clinical trials. Predictive testing is not considered appropriate for asymptomatic at-risk individuals younger than age 18 years. Prenatal testing by molecular genetic testing and preimplantation genetic testing are possible.

Suggestive Findings

Huntington disease (HD) should be suspected in individuals with any of the following:

• Progressive motor disability featuring chorea. Voluntary movement may also be affected.
• Mental disturbances including cognitive decline, changes in personality, and/or depression
• Family history consistent with autosomal dominant inheritance

Note: The appearance and sequence of motor, cognitive, and psychiatric disturbances can be variable in HD (see Clinical Description).

Establishing the Diagnosis

The diagnosis of HD is established in a proband with clinical signs and symptoms of HD by the identification of a heterozygous abnormal CAG trinucleotide repeat expansion in HTT by molecular genetic testing (see Table 1).

Note: Pathogenic (CAG)_n repeat expansions in HTT cannot currently be detected by clinical sequence-based multigene panels, exome sequencing, or genome sequencing.

CAG repeat sizes

• Normal. 26 or fewer CAG repeats
• Intermediate. Range from 27 to 35 CAG repeats. An individual with an allele in this range is not at risk of developing symptoms of HD but, because of instability in the CAG tract, may be at risk of having a child with an allele in the HD-causing range [Semaka et al 2006]. Risk estimates for germline CAG expansion have been established [Semaka et al 2013a, Semaka & Hayden 2014].
• Pathogenic HD-causing alleles. 36 or more CAG repeats. Persons who have an HD-causing allele are considered at risk of developing HD in their lifetime. HD-causing alleles are further classified as:
  • Reduced-penetrance HD-causing alleles. Range from 36 to 39 CAG repeats. An individual with an allele in this range is at risk for HD but may not develop symptoms. Elderly asymptomatic individuals with CAG repeats in this range are common [Kay et al 2016].
  • Full-penetrance HD-causing alleles. 40 or more CAG repeats. Alleles of this size are associated with development of HD with increased certainty assuming a normal life span.

Molecular genetic testing relies on targeted analysis to characterize the number of HTT CAG repeats.

Note: For comprehensive recommendations pertaining to predictive genetic testing for HD, see Genetic Counseling and MacLeod et al [2013].

Clinical Description

During the prodromal phase of Huntington disease (HD) individuals may have subtle changes in motor skills, cognition, and personality (see Figure 1) [Tabrizi et al 2013, Ross et al 2014, Liu et al 2015]. These subtle changes can occur as early as 15-20 years prior to the clinical onset of manifest HD.

Figure 1.

Natural history of Huntington disease (HD). Presymptomatic individuals are free from signs and symptoms of HD. During the prodromal phase, subtle signs and symptoms may be present prior to the diagnosis of HD, which is usually based on motor symptoms. (more...)

Reilmann et al [2014] present guidelines for the diagnostic criteria of presymptomatic, prodromal, and manifest HD; see Table 2. This table can be used to place individuals into different diagnostic categories, which may have clinical management implications over time. For example, awareness of presymptomatic and prodromal HD may allow for preventive (rather than symptomatic) therapies. Note the clear differentiation of genetically confirmed HD in the classification system.

The mean age of onset for HD is approximately 45 years [Bates et al 2015]. About two thirds of affected individuals first present with neurologic manifestations; others present with psychiatric changes. In the early stages following diagnosis, manifestations include subtle changes in eye movements, coordination, minor involuntary movements, difficulty in mental planning, and often a depressed or irritable mood (see Table 3). Affected individuals are usually able to perform most of their ordinary activities and to continue working [Ross et al 2014, Bates et al 2015].

In approximately 25% of individuals with HD, the onset is delayed until after age 50 years, with some after age 70 years. These individuals have chorea, gait disturbances, and dysphagia, but a more prolonged and benign course than the typical individual.

In the next stage, chorea becomes more prominent, voluntary activity becomes increasingly difficult, and dysarthria and dysphagia worsen. Most individuals are forced to give up their employment and depend increasingly on others for help, although they are still able to maintain a considerable degree of personal independence. The impairment is usually considerable, sometimes with intermittent outbursts of aggressive behaviors and social disinhibition.

In late stages of HD, motor disability becomes severe and the individual is often totally dependent, mute, and incontinent. The median survival time after onset is 15 to 18 years (range: 5 to >25 years). The average age at death is 54 to 55 years [Bates et al 2015].

Abnormalities of movement. Disturbances of both involuntary and voluntary movements occur in individuals with HD. Chorea, an involuntary movement disorder consisting of nonrepetitive, nonperiodic jerking of limbs, face, or trunk, is the major sign of the disease. Chorea is present in more than 90% of individuals, and typically increases in severity during the first ten years. The choreic movements are continuously present during waking hours, cannot be suppressed voluntarily, and are worsened by stress.

With advancing disease duration, other involuntary movements such as bradykinesia, rigidity, and dystonia occur. Impairment in voluntary motor function is an early sign. Affected individuals and their families describe clumsiness in common daily activities. Motor speed, fine motor control, and gait are affected. Oculomotor disturbances occur early and worsen progressively. Difficulty in initiating ocular saccades, slow and hypometric saccades, and problems in gaze fixation may be seen in up to 75% of symptomatic individuals [Blekher et al 2006, Golding et al 2006]. Dysarthria occurs early and is common. Dysphagia occurs in the late stages. Hyperreflexia occurs early in 90% of individuals, while clonus and extensor plantar responses occur late and less frequently.

Abnormalities of cognition. A global and progressive decline in cognitive capabilities occurs in all individuals with HD. Cognitive changes include forgetfulness, slowness of thought processes, impaired visuospatial abilities, and impaired ability to manipulate acquired knowledge. Several studies have identified subtle but definite cognitive deficits prior to the onset of motor symptoms [Bourne et al 2006, Montoya et al 2006, Paulsen et al 2008, Tabrizi et al 2009, Rupp et al 2010]. The initial changes often involve loss of mental flexibility and impairment of executive functions such as mental planning and organization of sequential activities.

Memory deficits with greater impairment for retrieval of information occur early, but verbal cues, priming, and sufficient time may lead to partial or correct recall. Early in the disease the memory deficits in HD are usually much less severe than in Alzheimer disease.

The overall cognitive and behavioral syndrome in individuals with HD is more similar to frontotemporal dementia than to Alzheimer disease. Attention and concentration are involved early [Peinemann et al 2005], resulting in easy distractibility. Language functions are relatively preserved, but a diminished level of syntactic complexity, cortical speech abnormalities, paraphasic errors, and word-finding difficulties are common in late stages.

Neuropsychologic testing reveals impaired visuospatial abilities, particularly in late stages of the disease. Lack of awareness, especially of one's own disabilities, is common [Ho et al 2006, Bates et al 2015].

Psychiatric disturbances. Individuals with HD develop significant personality changes, affective psychosis, or schizophrenic psychosis [Rosenblatt 2007]. Prior to onset of HD, they tend to score high on measures of depression, hostility, obsessive-compulsiveness, anxiety, and psychoticism [Duff et al 2007]. Unlike the progressive cognitive and motor disturbances, the psychiatric changes tend not to progress with disease severity [Epping et al 2016]. Behavioral disturbances such as intermittent explosiveness, apathy, aggression, alcohol abuse, sexual dysfunction and deviations, and increased appetite are frequent. Delusions, often paranoid, are common. Hallucinations are less common.

Depression and suicide risk. The incidence of depression in preclinical and symptomatic individuals is more than twice that in the general population [Paulsen et al 2005b, Marshall et al 2007]. The etiology of depression in HD is unclear; it may be a pathologic rather than a psychological consequence of having the disease [Slaughter et al 2001, Pouladi et al 2009]. Suicide and suicide ideation are common in persons with HD, but the incidence rate changes with disease course and predictive testing results [Larsson et al 2006, Robins Wahlin 2007, van Duijn et al 2018]. The critical periods for suicide risk were found to be just prior to receiving a diagnosis and later, when affected individuals experience a loss of independence [Baliko et al 2004, Paulsen et al 2005a, Eddy et al 2016].

Other. Persons with HD tend to have a lower body mass index than controls [Pratley et al 2000, Stoy & McKay 2000, Djoussé et al 2002, Robbins et al 2006], which may be related to altered metabolism [Duan et al 2014] and could represent a biomarker of clinical progression [van der Burg et al 2017]. Individuals with HD also demonstrate disturbed cholesterol metabolism [Valenza & Cattaneo 2006, Wang et al 2014]. It is also common for persons with HD to demonstrate increased appetite and energy expenditure [Pratley et al 2000, Trejo et al 2004, Gaba et al 2005].

Sleep and circadian rhythms are disrupted in individuals with HD [Goodman & Barker 2010, Morton 2013], possibly as a result of hypothalamic dysfunction [Petersén & Björkqvist 2006] and/or alterations in melatonin secretion [Kalliolia et al 2014]. Insomnia and daytime somnolence may also be present, although this is more commonly due to psychiatric changes, depression, or chorea [Videnovic et al 2009].

Neuropathology. The primary neuropathologic feature of HD is degeneration of neurons in the caudate and putamen as well as the cerebral cortex [Waldvogel et al 2015]. The preferential degeneration of enkephalin-containing, medium spiny neurons of the indirect pathway of movement control in the basal ganglia provides the neurobiologic basis for chorea [Galvan et al 2012]. The additional loss of substance P-containing medium spiny neurons of the direct pathway results in akinesia and dystonia [Galvan et al 2012]. There is also evidence for loss of neurons in the globus pallidus, subthalamic nucleus, thalamus, hypothalamus, substantia nigra, and hippocampus [Vonsattel et al 1985, Vonsattel & DiFiglia 1998, Heinsen et al 1999, Petersén et al 2005, Guo et al 2012, Domínguez et al 2013, Singh-Bains et al 2016]. Region-specific patterns of neuronal loss in the basal ganglia and cortex may underlie the most evident symptoms in affected individuals and could contribute to the phenotypic variability among individuals [Thu et al 2010, Hadzi et al 2012, Kim et al 2014, Waldvogel et al 2015, Mehrabi et al 2016]. Pathology is also observed in peripheral tissues [Björkqvist et al 2008, van der Burg et al 2009].

Intraneuronal inclusions containing huntingtin, the protein expressed from HTT, are also a prominent neuropathologic feature of the disease. However, the expression of the huntingtin protein and the pattern and timing of huntingtin-containing inclusions in the brain do not correlate with the selective degeneration of the disease and are not believed to be primary determinants of pathology [Kuemmerle et al 1999, Michalik & Van Broeckhoven 2003, Arrasate et al 2004, Slow et al 2005, Slow et al 2006].

Neuroimaging. Imaging studies provide additional support for the clinical diagnosis of HD and are valuable tools for studying progression of the disease [Biglan et al 2009, Paulsen 2009, Tabrizi et al 2011, Tabrizi et al 2012, Tabrizi et al 2013]. In addition to significant striatal atrophy in symptomatic individuals, regional and whole-brain gray and white matter changes have been detected [Majid et al 2011, Tabrizi et al 2011, Tabrizi et al 2012, Tabrizi et al 2013]. Furthermore, MRI studies have revealed progressive gray and white matter atrophy many years prior to predicted disease onset [Tabrizi et al 2011, Tabrizi et al 2012, Tabrizi et al 2013]. Numerous studies in recent years have used neuroimaging to elucidate the clinical progression of HD, with the specific interest of using these objective measures in clinical trials for testing efficacy of experimental therapeutics [Tabrizi et al 2012, Tabrizi et al 2013].

Juvenile HD is defined by the onset of symptoms before age 20 years and accounts for 5%-10% of individuals with HD [Gonzalez-Alegre & Afifi 2006, Quarrell et al 2013]. The motor, cognitive, and psychiatric disturbances observed in adult HD are also observed in juvenile HD, but the clinical presentation of these disturbances is different. Severe mental deterioration, prominent motor and cerebellar symptoms, speech and language delay, and rapid decline are also characteristic of juvenile HD [Nance & Myers 2001, Gonzalez-Alegre & Afifi 2006, Squitieri et al 2006, Yoon et al 2006]. Epileptic seizures, unique to the youngest-onset group, are present in 30%-50% of those with onset of HD before age ten years [Gonzalez-Alegre & Afifi 2006].

In teenagers, symptoms are more similar to adult HD, in which chorea and severe behavioral disturbances are common initial manifestations [Nance & Myers 2001].

Intermediate alleles (IA). An individual with a CAG repeat in the 27-35 range is not believed to be at risk of developing HD but, because of instability in the CAG tract, may be at risk of having a child with an allele in the pathogenic CAG range [Semaka et al 2006, Kay et al 2018]. Limited data suggest that individuals with IAs may exhibit behavioral changes as well as motor and cognitive impairments, although more research is required in this regard [Killoran et al 2013, Cubo et al 2016].

Genotype-Phenotype Correlations

A significant inverse correlation exists between the number of CAG repeats and the age of onset of HD [Langbehn et al 2004, Langbehn et al 2010]. See Molecular Genetics.

• Individuals with adult onset of symptoms usually have an HTT allele with CAG repeats ranging from 36 to 55.
• Individuals with juvenile onset of symptoms usually have an HTT allele with CAG repeats greater than 60.
• Intermediate alleles (ranging from 27 to 35 CAG repeats) usually have not been associated with disease but are prone to CAG repeat instability [Semaka et al 2013b].

For data on the age-specific likelihood of onset by trinucleotide repeat size, see ubc.ca (pdf).

In addition to age at clinical onset, CAG repeat length has also been shown to predict age at death, but not the duration of the illness [Keum et al 2016].

The rate of deterioration of motor, cognitive, and functional measures increases with larger CAG repeat sizes [Aziz et al 2009, Chao et al 2017].

The progression of behavioral symptoms appears not to be related to repeat size [Ravina et al 2008].

Homozygotes for fully penetrant HD alleles appear to have a similar age of onset to heterozygotes, but may exhibit an accelerated rate of disease progression [Squitieri et al 2011, Lee et al 2012].

A significant negative correlation also exists between CAG size and variability of onset, in which more variability in the late age of onset is associated with smaller CAG sizes, suggesting that non-CAG modifiers may have a greater effect at lower CAG sizes than at larger CAG sizes [Langbehn et al 2004, Gusella & Macdonald 2009]. On average, the CAG repeat size accounts for up to 70% of the variability in age of onset, with an estimated 10%-20% of the residual variability being accounted for by heritable factors [Li et al 2006, Gusella & Macdonald 2009]. Many genes at other loci have been shown to account for small amounts of this heritable portion of the variability [GeM-HD Consortium 2015].

Significant progress has been made in recent years in the identification of these additional genomic modifiers, both at the HTT locus and throughout the genome.

• Cis-acting factors. The most common CAG repeat tract (>95% of alleles) has a CAA interruption in the penultimate repeat [(CAG)n-CAA-CAG]. Uninterrupted CAG repeats [(CAG)n] are associated with decreased age of onset in HD and increased somatic instability of the repeat [Ciosi et al 2019, GeM-HD Consortium 2019, Wright et al 2019] (GeM-HD 2019 full text). These findings suggest that uninterrupted CAG length is more predictive than polyglutamine length in estimating HD age of onset.
• Trans-acting factors. Genome-wide association studies have identified other candidate modifier genes for HD [GeM-HD Consortium 2015, Moss et al 2017]. These analyses have shown the important role of biologic pathways involved in DNA repair, mitochondrial fission, and oxidoreductase activity with regard to this phenotype, and have identified candidate modifier genes for future study (e.g., FAN1, MLH1, MTMR10, MSH3, and RRM2B).

Penetrance

Alleles with 36 to 39 CAG repeats are considered HD-causing alleles, but exhibit incomplete penetrance. Elderly asymptomatic individuals with CAG repeats in this range are common [Kay et al 2016].

Disease risk varies for the common [(CAG)n-CAA-CAG] interrupted repeat, observed in more than 95% of alleles, and the rare [(CAG)n] uninterrupted repeat, observed in about 1% of alleles [Ciosi et al 2019, GeM-HD Consortium 2019, Wright et al 2019] (GeM-HD 2019 full text):

• 36-39 repeats. Approximately one third of symptomatic individuals have a pure [(CAG)n] repeat.
• 36 and 37 repeats. The majority of symptomatic individuals have a pure [(CAG)n] repeat.

The loss of the CAA repeat has been termed the loss of interruption (LOI) variant [Wright et al 2019] and will be useful in modifying the probability of disease in individuals with 36-39 CAG repeats.

Alleles that contain more than 40 CAG repeats are completely penetrant. No asymptomatic elderly individuals with alleles of more than 40 CAG repeats have been reported.

Anticipation

Anticipation, the phenomenon in which increasing disease severity or decreasing age of onset is observed in successive generations, is known to occur in HD. Anticipation occurs far more commonly in paternal transmission of the mutated allele. The phenomenon of anticipation arises from instability of the CAG repeat during spermatogenesis [Semaka et al 2013a]. Large expansions (i.e., an increase in allele size of >7 CAG repeats) occur almost exclusively through paternal transmission. Most often children with juvenile-onset disease inherit the expanded allele from their fathers, although on occasion they inherit it from their mothers [Nahhas et al 2005].

Nomenclature

In the pre-molecular-genetic era, there were many different names for chorea, including St. Vitus's dance and Sydenham's chorea.

Juvenile HD, or childhood-onset HD, was previously called the Westphal variant of HD.

Individuals who do not yet show symptoms are in the premanifest phase of HD. Individuals who have been diagnosed with chorea and/or other validated signs of the disorder have manifest HD.

Prevalence

HD prevalence varies across world regions. Populations of European ancestry display an average prevalence of 9.71:100,000 [Rawlins et al 2016], but estimates as high as 17:100,000 have been reported [Fisher & Hayden 2014, Baig et al 2016]. In contrast, HD appears much less frequently in Japan, China, Korea, and Finland, as well as in indigenous African populations from South Africa, with estimated prevalence values ranging from 0.1:100,000 to 2:100,000 [Pringsheim et al 2012, Sipilä et al 2015, Xu & Wu 2015].

Individuals living in the Lake Maracaibo region of Venezuela are believed to have the highest prevalence of HD in the world [Wexler et al 2004].

The uneven distribution of HD is at least partially explained by the distribution of specific predisposing alleles and haplotypes in the general population of these ethnic groups [Warby et al 2009, Warby et al 2011, Kay et al 2018]. For example, a recent study of 15 diverse global populations demonstrated that the mean CAG size in a population, as well as intermediate allele frequency, correlates with HD prevalence and contributes to differences in disease prevalence across major ancestry groups [Kay et al 2018].

Reduced-penetrance HTT alleles (see Establishing the Diagnosis, CAG repeat sizes) have recently been shown to occur at a high frequency in the general population, with as many as one in 400 individuals having these alleles – although the penetrance rate was determined to be lower than previously reported (i.e., 0.2%-2% for 36-38 CAG alleles) [Kay et al 2016].

Evaluations Following Initial Diagnosis

To establish the extent of disease and needs in an individual diagnosed with Huntington disease (HD), the evaluations summarized in this section (if not performed as part of the evaluation that led to the diagnosis) are recommended:

• Physical examination
• Neurologic assessment
• Assessment of the full range of motor, cognitive, and psychiatric symptoms associated with HD. Among a range of clinical scoring systems that have been described, the Unified Huntington's Disease Rating Scale (UHDRS) provides a reliable and consistent assessment of the clinical features and progression of HD.
• Consultation with a clinical geneticist and/or genetic counselor

Treatment of Manifestations

Pharmacologic therapy is limited to symptomatic treatment [Mestre et al 2009, Killoran & Biglan 2014].

• Choreic movements can be partially suppressed by typical (haloperidol) and atypical (olanzapine) neuroleptics; benzodiazepines; or the monoamine-depleting agent tetrabenazine [de Tommaso et al 2005, Bonelli & Wenning 2006, Huntington Study Group 2006]. Tetrabenazine can be effective as an antichoreic drug; however, its use is associated with severe adverse effects including extrapyramidal symptoms. Deutetrabenazine, a deuterated analog of tetrabenazine, has been modified by deuterium atom substitutions at specific sites on the molecule to increase half-life and systemic exposure [Stamler et al 2013]. These properties allow for less frequent dosing with fewer adverse effects [Frank et al 2016, Reilmann 2016].
• Anti-parkinsonian agents may ameliorate hypokinesia and rigidity, but may increase chorea.
• Psychiatric disturbances such as depression, psychotic symptoms, and outbursts of aggression generally respond well to psychotropic drugs or some types of anti-seizure medication.
• Valproic acid has improved myoclonic hyperkinesia in Huntington disease [Saft et al 2006].

Supportive care with attention to nursing, diet, special equipment, and eligibility for state and federal benefits is much appreciated by individuals with HD and their families. Numerous social challenges beset individuals with HD and their families; practical help, emotional support, and counseling can provide relief [Williams et al 2009].

Prevention of Secondary Complications

Significant secondary complications of HD include the following:

• The complications typically observed with any individual requiring long-term supportive care
• The side effects associated with various pharmacologic treatments. Drug side effects are dependent on a variety of factors including the compound involved, the dosage, and the individual; with the medications typically used in HD, side effects may include depression, sedation, nausea, restlessness, headache, neutropenia, and tardive dyskinesia. For some individuals, the side effects of certain therapeutics may be worse than the symptoms; such individuals would benefit from being removed from the treatment, having the dose reduced, or being "rested" regularly from the treatment. Current medications used to treat chorea are particularly prone to significant side effects. Individuals with mild-to-moderate chorea may be better assisted with nonpharmacologic therapies such as movement training and speech therapy.
• Depression. Standard treatment is appropriate when indicated [Paulsen et al 2005b, Phillips et al 2008].

Surveillance

Regular evaluations should be made to address the appearance and severity of chorea, rigidity, gait abnormalities, depression, behavioral changes, and cognitive decline [Anderson & Marshall 2005, Skirton 2005].

The Behavior Observation Scale Huntington (BOSH) is a scale developed for the rapid and longitudinal assessment of functional abilities of persons with HD in a nursing home environment [Timman et al 2005]. For longitudinal studies, the Unified Huntington's Disease Rating Scale (UHDRS) is used [Huntington Study Group 1996, Siesling et al 1998, Youssov et al 2013]. The total functional capacity (TFC) scale is used to describe the progression of HD, the level of functioning, and requirements for additional caregiver aid.

Agents/Circumstances to Avoid

L-dopa-containing compounds may increase chorea.

Alcohol and smoking are discouraged.

Evaluation of Relatives at Risk

See Genetic Counseling for issues related to testing of at-risk relatives for genetic counseling purposes.

Therapies Under Investigation

A wide range of potential therapeutics are under investigation in both animal models of HD and human clinical trials [Wild & Tabrizi 2014]. This diversity reflects the variety of cellular pathways known to be perturbed in HD [Bonelli et al 2004, Rego & de Almeida 2005, Borrell-Pagès et al 2006, Graham et al 2006, Bonelli & Hofmann 2007].

• Pharmacologic agents being investigated include inhibitors of: apoptosis, excitotoxicity, huntingtin aggregation, huntingtin proteolysis, huntingtin phosphorylation, inflammation, oxidative damage, phosphodiesterase activity, histone deacetylase, and transglutaminase activity; as well as compounds that modulate mitochondrial function, chaperone activity, transcription, and neurotrophic support.
• Therapeutics that have shown improvements in preclinical animal models of HD and have been advanced to clinical trials include minocycline, sodium butyrate, essential fatty acids, racemide, creatine, cystamine, riluzole, memantine, resveratrol, cannabis extract (THC and CBD), coenzyme Q₁₀, and a phosphodiesterase 10a inhibitor [Bender et al 2005, Puri et al 2005, Bonelli & Wenning 2006, Ondo et al 2007, Okamoto et al 2009, Huntington Study Group DOMINO Investigators 2010, Hersch et al 2017, McGarry et al 2017]. Notably, many of these therapeutic agents have failed to meet clinical endpoints and demonstrate efficacy in modifying clinical progression of HD. Experimental therapeutics including pridopidine, laquinimod, and a semaphorin-4D neutralizing antibody are still in clinical development.
• Gene-silencing approaches to target the cause of HD have been shown to be safe and efficacious in preclinical animal studies and are currently undergoing or on the verge of entering clinical trials. These include approaches using RNA interference (RNAi) or antisense oligonucleotides (ASOs) [Boudreau et al 2009, Pfister & Zamore 2009, Hu et al 2010, McBride et al 2011, Kordasiewicz et al 2012, Aronin & DiFiglia 2014, Dufour et al 2014, Stanek et al 2014, Pfister et al 2018]. These approaches either aim to silence all huntingtin expression in a nonselective manner [Boudreau et al 2009, McBride et al 2011, Kordasiewicz et al 2012] or are allele selective for only the mutated HTT allele [Gagnon et al 2010, Carroll et al 2011, Evers et al 2011, Skotte et al 2014, Southwell et al 2014, Datson et al 2017]. Allele selectivity can be achieved by targeting the expanded CAG tract [Gagnon et al 2010, Evers et al 2011, Datson et al 2017] or by targeting polymorphisms in linkage disequilibrium with the CAG expansion [Carroll et al 2011, Skotte et al 2014, Southwell et al 2014, Kay et al 2015, Southwell et al 2018]. Results from the first in-human Phase I/IIa clinical trial evaluating the HTT targeted ASO showed that IONIS-HTT_Rx (RG6042) was well tolerated at all doses tested and resulted in dose-dependent reductions of mHTT in cerebrospinal fluid (CSF) [Tabrizi et al 2019].
• Cell transplantation studies in HD have shown variable results with small numbers of individuals [Furtado et al 2005, Bachoud-Lévi et al 2006, Farrington et al 2006, Dunnett & Rosser 2007, Barker et al 2013]; however, additional larger studies are under way [Lopez et al 2014]. Moreover, the safety and efficacy of intravenously injected mesenchymal stem cells is currently being tested in a first-in-human clinical trial for individuals with HD (NCT02728115). Of concern, recent studies suggest that mutated huntingtin is capable of spreading into the allografted neural tissue [Cicchetti et al 2014].

Numerous human clinical trials are planned or under way for HD and are listed at huntingtonstudygroup.org. A number of drug trials have been completed and/or are ongoing.

Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for information on clinical studies for a wide range of diseases and conditions.

Other

Biomarker studies, such as TRACK-HD, PREDICT-HD, and ENROLL-HD, have been conducted to identify early changes in disease progression using imaging, clinical scales, and physiologic measurements [Scahill et al 2012, Ross et al 2014]. Longitudinal studies of persons at risk for HD have also been performed [Huntington Study Group PHAROS Investigators 2006, Paulsen et al 2006, Tabrizi et al 2012].

A number of candidate molecular biomarkers of disease onset and clinical progression have been assessed in HD patient cohorts, yet only a few have been validated. Mutated huntingtin levels in CSF have been shown to correlate with disease stage in HD [Southwell et al 2015, Wild et al 2015] and potentially reflect levels of mHTT in the brain [Southwell et al 2015]. Therefore, mHTT levels in CSF may provide a reliable biomarker of clinical progression and may provide a proxy measurement for HTT suppression in the brain for HTT-targeted clinical trials. Moreover, levels of neurofilament light chain in blood and CSF have been shown to be a potential prognostic biomarker of disease onset and clinical progression as well as regional brain atrophy in individuals with HD [Byrne et al 2017, Johnson et al 2018].

Children and adolescents living with a parent affected with HD, sometimes in very deprived conditions, can have special challenges. Referral to a local HD support group for educational material and needed psychological support is helpful (see Resources).

Donepezil, a drug used to treat Alzheimer disease, has not improved motor or cognitive function in HD [Cubo et al 2006].

Mode of Inheritance

Huntington disease (HD) is inherited in an autosomal dominant manner.

Risk to Family Members

Parents of a proband

• Most individuals diagnosed with HD have an affected parent.
• The family history of some individuals diagnosed with HD may appear to be negative for one of the following reasons:
  • Failure to recognize the disorder in family members
  • Early death of the parent before the onset of symptoms
  • The presence of an intermediate allele (range: 27-35 CAG repeats) or an HTT allele with reduced penetrance (range: 36-39 CAG repeats) in an asymptomatic parent (See Offspring of a proband.)
  • Late onset of the disease in the affected parent
• Molecular genetic testing is recommended for the parents of a proband who appears to represent a simplex case (i.e., a single occurrence in a family).

Sibs of a proband. The risk to the sibs of a proband depends on the genetic status of the proband's parents:

• If a parent has an HTT allele with CAG length of 40 or greater, the risk to the sibs of inheriting a full-penetrance HD-causing allele is 50%.
• If a parent has an HTT allele with reduced penetrance (36-39 CAG repeats), the risk to the sibs of inheriting a pathogenic HD-causing allele (of either reduced or full penetrance) is 50% (see Anticipation).
• If a parent has an intermediate HTT allele (27-35 CAG repeats), the risk to the sibs of inheriting a CAG expansion greater than 35 repeats or a "new HD-causing allele" depends on a variety of factors, including the following (see also Anticipation):
  • The CAG size of the allele. Larger CAG sizes are more prone to expansion.
    CAG size-specific estimates for repeat instability in sperm have been reported to enable genetic counselors to provide more accurate risk assessment for persons who receive an intermediate allele predictive test result [Hendricks et al 2009, Semaka et al 2013a, Semaka & Hayden 2014]. While all intermediate CAG repeat sizes were shown to have the possibility of expansion, the probability of expansion increases dramatically with increasing CAG size; approximately 21% of 35 CAG alleles expanded into the disease-associated range. Evidence-based genetic counseling implications for intermediate allele predictive test results have been published by Semaka & Hayden [2014].
  • The sex and age of the transmitting parent. Paternally inherited intermediate alleles are more prone to CAG expansion than maternally inherited intermediate alleles; maternal expansions are extremely rare [Semaka et al 2015]. Expanded intermediate alleles are preferentially transmitted by males with advanced paternal age.
  • The DNA sequence in cis configuration with the CAG expansion. CAG tracts interrupted with CAA and CCG trinucleotides are more stable.

Offspring of a proband

• At conception, each child of an individual with HD as a result of heterozygosity for a CAG repeat expansion in HTT has a 50% chance of inheriting the HD-causing allele. Offspring who inherit a:
  • Reduced-penetrance allele (36-39 CAG repeats) are at risk for HD but may not develop symptoms (see Penetrance);
  • Full-penetrance allele (40 or more CAG repeats) are at risk of developing HD with increased certainty assuming a normal life span.
• Each child of an affected individual who is homozygous for CAG repeat expansion in HTT will inherit an HD-causing allele.

Other family members. The risk to other family members depends on the genetic status of the proband's parents: if a parent is affected or has a CAG expansion in HTT, the parent's family members are at risk.

Related Genetic Counseling Issues

Predictive testing (i.e., testing of asymptomatic at-risk individuals). Testing of asymptomatic adults at risk for HD is possible. Testing for the pathogenic variant in the absence of definite symptoms of the disease is predictive testing. Such testing is not useful in accurately predicting age of onset, severity, type of symptoms, or rate of progression in asymptomatic individuals. However, data reported by Langbehn et al [2004] and Langbehn et al [2010] concerning the likelihood that an individual with a particular size of CAG repeat will be affected by a specific age may be useful. Current diagnostic assays are only capable of measuring CAG length up to the penultimate CAA in the canonic sequence. In the presence of the loss of interruption variant (CAA to CAG), current diagnostic methods would underestimate CAG length by two CAG repeats. This does not affect the majority of individuals with HD [Wright et al 2019]. See Supplementary Tables at ubc.ca (pdf). When testing at-risk individuals for HD, it is helpful to test for the CAG expansion in HTT in an affected family member to confirm that the disorder in the family is HD.

• At-risk asymptomatic adult family members may seek testing in order to make personal decisions regarding reproduction, financial matters, and career planning. Asymptomatic individuals at risk may also be eligible to participate in clinical trials. Others may have different motivations including simply the "need to know." Testing of asymptomatic at-risk adult family members usually involves pretest interviews in which the motives for requesting the test, the individual's knowledge of HD, the possible impact of positive and negative test results, and neurologic status are assessed. Those seeking testing should be counseled about problems they may encounter with regard to health, life, and disability insurance coverage, employment and educational discrimination, and changes in social and family interaction. Interestingly, a study has found that genetic testing does not increase the risk for discrimination; perceived genetic discrimination is more likely due to the family history of HD regardless of gene status, rather than due to the specific results of the HD genetic test [Bombard et al 2009]. Other issues to consider include implications for the at-risk status of other family members [Bombard et al 2012]. Depression and suicide ideation are issues to be addressed as part of the predictive testing program for HD [Robins Wahlin et al 2000, Robins Wahlin 2007]. Informed consent should be obtained and records kept confidential. Individuals with a mutated allele need arrangements for long-term follow up and evaluations.
• Short-term follow up of the participants in the Canadian Predictive Testing Program has revealed that predictive testing for HD may maintain or even improve the psychological well-being of at-risk individuals even though some had negative experiences. About 10% of the group who were determined to be at decreased risk had serious difficulties adapting to their new status. The major issue for these individuals is the realization that they are facing an unplanned future. Overall, the demand for testing of at-risk asymptomatic adults has been lower than expected in studies conducted before the availability of direct molecular genetic testing. Consistent with use of medical services and genetic testing in general, women are more likely than men to undergo predictive testing for HD [Taylor 2005, Baig et al 2016].
• In their study of psychological distress in the partners of asymptomatic individuals who had inherited an HD-causing allele, Decruyenaere et al [2005] found that partners have at least as much distress as the individuals found to have the HD-causing allele, yet their grief tends to be "disenfranchised" or not socially recognized.

Predictive testing in minors (i.e., testing of asymptomatic at-risk individuals younger than age 18 years)

• For asymptomatic minors at risk for adult-onset conditions for which early treatment would have no beneficial effect on disease morbidity and mortality, predictive genetic testing is considered inappropriate, primarily because it negates the autonomy of the child with no compelling benefit. Further, concern exists regarding the potential unhealthy adverse effects that such information may have on family dynamics, the risk of discrimination and stigmatization in the future, and the anxiety that such information may cause.
• For more information, see the National Society of Genetic Counselors position statement on genetic testing of minors for adult-onset conditions and the American Academy of Pediatrics and American College of Medical Genetics and Genomics policy statement: ethical and policy issues in genetic testing and screening of children.

In a family with an established diagnosis of HD, it is appropriate to consider testing of symptomatic individuals regardless of age.

Considerations in families with an apparent de novo pathogenic variant. When neither parent has an HD-causing HTT allele (>35 CAG repeats) or an intermediate allele (27-35 repeats), nonmedical explanations including alternate paternity or maternity (e.g., with assisted reproduction) and undisclosed adoption could be explored.

Family planning

• The optimal time for determination of genetic risk and discussion of the availability of prenatal/preimplantation genetic testing is before pregnancy.
• Similarly, decisions about testing to determine the genetic status of at-risk asymptomatic family members are best made before pregnancy.

Prenatal Testing and Preimplantation Genetic Testing

For fetuses at 50% risk. If the presence of an HD-causing HTT allele has been confirmed in the affected parent or in an affected relative of the at-risk parent, prenatal testing for a pregnancy at increased risk is possible.

Preimplantation genetic testing (PGT) may be an option for families in which an HD-causing HTT allele has been identified in an affected family member. Existing PGT exclusion protocols allow for testing of the embryo for couples in an at-risk family who do not wish to undergo presymptomatic testing for the HD-causing allele themselves [Sermon et al 2002, Stern et al 2002, Moutou et al 2004, Jasper et al 2006]. Counseling and ethical issues affecting PGT for HD are discussed by Asscher & Koops [2010].

Differences in perspective may exist among medical professionals and within families regarding the use of prenatal testing when the testing is being considered for the purpose of pregnancy termination or for early diagnosis. While most centers would consider use of prenatal testing to be a personal decision, discussion of these issues may be helpful.

Molecular Pathogenesis

HTT encodes the huntingtin protein. A CAG trinucleotide repeat expansion in exon one of HTT is translated into an uninterrupted stretch of glutamine residues in huntingtin. This polyglutamine expansion in huntingtin elicits toxic effects by dysregulating vital cellular processes, which ultimately leads to cell death.

Of note, huntingtin acts as a scaffold to facilitate several essential functions in the cell, including cytoskeletal dynamics, endocytosis, vesicular trafficking (BDNF), energy metabolism, protein turnover, and gene expression (transcription and RNA processing). In the presence of a CAG expansion, many of its roles are disrupted, likely contributing to the disease phenotype [Saudou & Humbert 2016].

Mechanism of disease causation. The primary mechanism is gain of function; however, many studies support loss of function.

Methods to characterize HTT CAG repeats. Due to the technical challenges of detecting and sizing HTT CAG trinucleotide repeat expansions, multiple methods may be needed to rule out or detect CAG repeat expansion (see Table 6). Most repeats may be detected by traditional PCR. However, detection of apparent homozygosity for a normal CAG repeat does not rule out the presence of a very large expanded CAG repeat. Thus, testing by triplet-primed PCR (TP-PCR) or Southern blotting may be required. In addition, somatic and germline instability of expanded repeats must be considered.

Author Notes

Booklets available through the Huntington Society of Canada:

• Loss and Grief: Coping with the Death of a Loved One and with Other Losses Related to Huntington Disease
• A Physician's Guide to the Management of Huntington Disease (3rd edition)
• Caregiver's Handbook for Advanced Stages of Huntington Disease
• Juvenile Huntington Disease: A Resource for Families, Health Professionals and Caregivers
• Understanding Behaviour in Huntington Disease: A Guide for Professionals (3rd edition)
• Personal Perspectives on Genetic Testing for Huntington Disease
• Understanding Huntington Disease: A Resource for Families

Author History

Nicholas S Caron, PhD (2018-present)
Rona K Graham, PhD; University of Sherbrooke, Quebec (2007-2018)
Brendan Haigh, PhD; University of British Columbia (1998-2007)
Michael R Hayden, MB, ChB, PhD, FRCP(C), FRSC (1998-present)
Mahbubul Huq, PhD; University of British Columbia (1998-2007)
Simon C Warby, PhD; University of Montreal (2007-2018)
Galen EB Wright, PhD (2018-present)

Revision History

• 11 June 2020 (sw) Comprehensive update posted live
• 5 July 2018 (sw) Comprehensive update posted live
• 11 December 2014 (me) Comprehensive update posted live
• 22 April 2010 (me) Comprehensive update posted live
• 19 July 2007 (me) Comprehensive update posted live
• 30 August 2005 (cd) Revision: correction of CAG repeat ranges
• 15 February 2005 (me) Comprehensive update posted live
• 25 May 2004 (cd) Revisions
• 23 October 1998 (pb) Review posted live
• 16 May 1998 (mh) Original submission

Published Guidelines / Consensus Statements

• American College of Medical Genetics/American Society of Human Genetics Huntington Disease Genetic Testing Working Group (1998) Laboratory guidelines for Huntington disease genetic testing. Am J Hum Genet 62:1243-7. [PMC free article] [PubMed]
• Committee on Bioethics, Committee on Genetics, and American College of Medical Genetics and Genomics Social, Ethical, Legal Issues Committee. Ethical and policy issues in genetic testing and screening of children. Available online. 2013. Accessed 12-30-22.
• International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea (1994) Guidelines for the molecular genetics predictive test in Huntington's disease. Neurology 44:1533-6. [PubMed]
• International Huntington Association and World Federation of Neurology. Guidelines for the molecular genetic predictive test in Huntington's disease. Available online. 1994. Accessed 12-30-22.
• National Society of Genetic Counselors. Position statement on genetic testing of minors for adult-onset conditions. Available online. 2018. Accessed 12-30-22.
• World Federation of Neurology Research Committee Research Group on Huntington's Chorea (1989) Ethical issues policy statement on Huntington's chorea molecular genetics predictive test. J Neurol Sci 94:327-32. [PubMed]

Literature Cited

• Anderson KE, Marshall FJ. Behavioral symptoms associated with Huntington's disease. Adv Neurol. 2005;96:197–208. [PubMed: 16383221]
• Aronin N, DiFiglia M. Huntingtin-lowering strategies in Huntington's disease: antisense oligonucleotides, small RNAs, and gene editing. Mov Disord. 2014;29:1455–61. [PubMed: 25164989]
• Arrasate M, Mitra S, Schweitzer ES, Segal MR, Finkbeiner S. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature. 2004;431:805–10. [PubMed: 15483602]
• Asscher E, Koops B-J. The right not to know and preimplantation genetic diagnosis for Huntington's disease. J Med Ethics. 2010;36:30–3. [PubMed: 20026690]
• Aziz NA, Jurgens CK, Landwehrmeyer GB, van Roon-Mom WMC, van Ommen JGB, Stijnen T, Roos RAC, et al. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease. Neurology. 2009;73:1280–5. [PubMed: 19776381]
• Bachoud-Lévi AC, Gaura V, Brugieres P, Lefaucheur JP, Boisse MF, Maison P, Baudic S, Ribeiro MJ, Bourdet C, Remy P, Cesaro P, Hantraye P, Peschanski M. Effect of fetal neural transplants in patients with Huntington's disease 6 years after surgery: a long-term follow-up study. Lancet Neurol. 2006;5:303–9. [PubMed: 16545746]
• Baig SS, Strong M, Rosser E, Taverner NV, Glew R, Miedzybrodzka Z, Clarke A, Craufurd D, Quarrell OW, et al. 22 years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction Consortium. Eur J Hum Genet. 2016;24:1396–402. [PMC free article: PMC5027682] [PubMed: 27165004]
• Baliko L, Csala B, Czopf J. Suicide in Hungarian Huntington's disease patients. Neuroepidemiology. 2004;23:258–60. [PubMed: 15316254]
• Barker RA, Mason SL, Harrower TP, Swain RA, Ho AK, Sahakian BJ, Mathur R, Elneil S, Thornton S, Hurrelbrink C, Armstrong RJ, Tyers P, Smith E, Carpenter A, Piccini P, Tai YF, Brooks DJ, Pavese N, Watts C, Pickard JD, Rosser AE, Dunnett SB, et al. The long-term safety and efficacy of bilateral transplantation of human fetal striatal tissue in patients with mild to moderate Huntington's disease. J Neurol Neurosurg Psychiatry. 2013;84:657–65. [PMC free article: PMC3646287] [PubMed: 23345280]
• Bates GP, Dorsey R, Gusella JF, Hayden MR, Kay C, Leavitt BR, Nance M, Ross CA, Scahill RI, Wetzel R, Wild EJ, Tabrizi SJ. Huntington disease. Nat Rev Dis Primers. 2015;1:15005. [PubMed: 27188817]
• Bean L, Bayrak-Toydemir P. American College of Medical Genetics and Genomics Standards and Guidelines for Clinical Genetics Laboratories, 2014 edition: technical standards and guidelines for Huntington disease. Genet Med. 2014;16:e2. [PubMed: 25356969]
• Bender A, Auer DP, Merl T, Reilmann R, Saemann P, Yassouridis A, Bender J, Weindl A, Dose M, Gasser T, Klopstock T. Creatine supplementation lowers brain glutamate levels in Huntington's disease. J Neurol. 2005;252:36–41. [PubMed: 15672208]
• Biglan KM, Ross CA, Langbehn DR, Aylward EH, Stout JC, Queller S, Carlozzi NE, Duff K, Beglinger LJ, Paulsen JS, et al. Motor abnormalities in premanifest persons with Huntington's disease: the PREDICT-HD study. Mov Disord. 2009;24:1763–72. [PMC free article: PMC3048804] [PubMed: 19562761]
• Björkqvist M, Wild EJ, Thiele J, Silvestroni A, Andre R, Lahiri N, Raibon E, Lee RV, Benn CL, Soulet D, Magnusson A, Woodman B, Landles C, Pouladi MA, Hayden MR, Khalili-Shirazi A, Lowdell MW, Brundin P, Bates GP, Leavitt BR, Möller T, Tabrizi SJ. A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease. J Exp Med. 2008;205:1869–77. [PMC free article: PMC2525598] [PubMed: 18625748]
• Blekher T, Johnson SA, Marshall J, White K, Hui S, Weaver M, Gray J, Yee R, Stout JC, Beristain X, Wojcieszek J, Foroud T. Saccades in presymptomatic and early stages of Huntington disease. Neurology. 2006;67:394–9. [PubMed: 16855205]
• Bombard Y, Palin J, Friedman JM, Veenstra G, Creighton S, Bottorff JL, Hayden MR, et al. Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease. Am J Med Genet B Neuropsychiatr Genet. 2012;159B:217–26. [PubMed: 22231990]
• Bombard Y, Veenstra G, Friedman JM, Creighton S, Currie L, Paulsen JS, Bottorff JL, Hayden MR, et al. Perceptions of genetic discrimination among people at risk for Huntington's disease: a cross sectional survey. BMJ. 2009;338:b2175. [PMC free article: PMC2694258] [PubMed: 19509425]
• Bonelli RM, Hofmann P. A systematic review of the treatment studies in Huntington's disease since 1990. Expert Opin Pharmacother. 2007;8:141–53. [PubMed: 17257085]
• Bonelli RM, Wenning GK. Pharmacological management of Huntington's disease: an evidence-based review. Curr Pharm Des. 2006;12:2701–20. [PubMed: 16842168]
• Bonelli RM, Wenning GK, Kapfhammer HP. Huntington's disease: present treatments and future therapeutic modalities. Int Clin Psychopharmacol. 2004;19:51–62. [PubMed: 15076012]
• Borrell-Pagès M, Zala D, Humbert S, Saudou F. Huntington's disease: from huntingtin function and dysfunction to therapeutic strategies. Cell Mol Life Sci. 2006;63:2642–60. [PubMed: 17041811]
• Boudreau RL, McBride JL, Martins I, Shen S, Xing Y, Carter BJ, Davidson BL. Nonallele-specific silencing of mutant and wild-type huntingtin demonstrates therapeutic efficacy in Huntington's disease mice. Mol Ther. 2009;17:1053–63. [PMC free article: PMC2835182] [PubMed: 19240687]
• Bourne C, Clayton C, Murch A, Grant J. Cognitive impairment and behavioural difficulties in patients with Huntington's disease. Nurs Stand. 2006;20:41–4. [PubMed: 16722121]
• Byrne LM, Rodrigues FB, Blennow K, Durr A, Leavitt BR, Roos RAC, Scahill RI, Tabrizi SJ, Zetterberg H, Langbehn D, Wild EJ. Neurofilament light protein in blood as a potential biomarker of neurodegeneration in Huntington's disease: a retrospective cohort analysis. Lancet Neurol. 2017;16:601–9. [PMC free article: PMC5507767] [PubMed: 28601473]
• Carroll JB, Warby SC, Southwell AL, Doty CN, Greenlee S, Skotte N, Hung G, Bennett CF, Freier SM, Hayden MR. Potent and selective antisense oligonucleotides targeting single-nucleotide polymorphisms in the Huntington disease gene / allele-specific silencing of mutant huntingtin. Mol Ther. 2011;19:2178–85. [PMC free article: PMC3242664] [PubMed: 21971427]
• Chao TK, Hu J, Pringsheim T. Risk factors for the onset and progression of Huntington disease. Neurotoxicology. 2017;61:79–99. [PubMed: 28111121]
• Cicchetti F, Lacroix S, Cisbani G, Vallières N, Saint-Pierre M, St-Amour I, Tolouei R, Skepper JN, Hauser RA, Mantovani D, Barker RA, Freeman TB. Mutant huntingtin is present in neuronal grafts in Huntington disease patients. Ann Neurol. 2014;76:31–42. [PubMed: 24798518]
• Ciosi M, Maxwell A, Cumming SA, Hensman Moss DJ, Alshammari AM, Flower MD, Durr A, Leavitt BR, Roos RAC, Holmans P, Jones L, Langbehn DR, Kwak S, Tabrizi SJ, Monckton DG, et al. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. EBioMedicine. 2019 Oct;48:568–80. [PMC free article: PMC6838430] [PubMed: 31607598]
• Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C, et al. Clinical manifestations of intermediate allele carriers in Huntington disease. Neurology. 2016;87:571–8. [PubMed: 27402890]
• Cubo E, Shannon KM, Tracy D, Jaglin JA, Bernard BA, Wuu J, Leurgans SE. Effect of donepezil on motor and cognitive function in Huntington disease. Neurology. 2006;67:1268–71. [PubMed: 17030764]
• Datson NA, González-Barriga A, Kourkouta E, Weij R, van de Giessen J, Mulders S, Kontkanen O, Heikkinen T, Lehtimäki K, van Deutekom JC. The expanded CAG repeat in the huntingtin gene as target for therapeutic RNA modulation throughout the HD mouse brain. PLoS One. 2017;12:e0171127. [PMC free article: PMC5300196] [PubMed: 28182673]
• Davis MY, Keene CD, Jayadev S, Bird T. The co-occurrence of Alzheimer's disease and Huntington's disease: a neuropathological study of 15 elderly Huntington's disease subjects. J Huntingtons Dis. 2014;3:209–17. [PubMed: 25062863]
• Decruyenaere M, Evers-Kiebooms G, Boogaerts A, Demyttenaere K, Dom R, Fryns JP. Partners of mutation-carriers for Huntington's disease: forgotten persons? Eur J Hum Genet. 2005;13:1077–85. [PubMed: 15999117]
• de Tommaso M, Di Fruscolo O, Sciruicchio V, Specchio N, Cormio C, De Caro MF, Livrea P. Efficacy of levetiracetam in Huntington disease. Clin Neuropharmacol. 2005;28:280–4. [PubMed: 16340384]
• Djoussé L, Knowlton B, Cupples LA, Marder K, Shoulson I, Myers RH. Weight loss in early stage of Huntington's disease. Neurology. 2002;59:1325–30. [PubMed: 12427878]
• Domínguez D JF, Egan GF, Gray MA, Poudel GR, Churchyard A, Chua P, Stout JC, Georgiou-Karistianis N. Multi-modal neuroimaging in premanifest and early Huntington's disease: 18 month longitudinal data from the IMAGE-HD study. PLoS One. 2013;8:e74131. [PMC free article: PMC3774648] [PubMed: 24066104]
• Duan W, Jiang M, Jin J. Metabolism in HD: still a relevant mechanism? Mov Disord. 2014;29:1366–74. [PMC free article: PMC4163071] [PubMed: 25124273]
• Duff K, Paulsen JS, Beglinger LJ, Langbehn DR, Stout JC, et al. Psychiatric symptoms in Huntington's disease before diagnosis: the predict-HD study. Biol Psychiatry. 2007;62:1341–6. [PubMed: 17481592]
• Dufour BD, Smith CA, Clark RL, Walker TR, McBride JL. Intrajugular vein delivery of AAV9-RNAi prevents neuropathological changes and weight loss in Huntington's disease mice. Mol Ther. 2014;22:797–810. [PMC free article: PMC3982495] [PubMed: 24390280]
• Dunnett SB, Rosser AE. Stem cell transplantation for Huntington's disease. Exp Neurol. 2007;203:279–92. [PubMed: 17208230]
• Eddy CM, Parkinson EG, Rickards HE. Changes in mental state and behaviour in Huntington's disease. Lancet Psychiatry. 2016;3:1079–86. [PubMed: 27663851]
• Epping EA, Kim JI, Craufurd D, Brashers-Krug TM, Anderson KE, McCusker E, Luther J, Long JD, Paulsen JS, et al. Longitudinal psychiatric symptoms in prodromal Huntington's disease: a decade of data. Am J Psychiatry. 2016;173:184–92. [PMC free article: PMC5465431] [PubMed: 26472629]
• Evers MM, Pepers BA, van Deutekom JC, Mulders SA, den Dunnen JT, Aartsma-Rus A, van Ommen GJ, van Roon-Mom WM. Targeting several CAG expansion diseases by a single antisense oligonucleotide. PLoS One. 2011;6:e24308. [PMC free article: PMC3164722] [PubMed: 21909428]
• Farrington M, Wreghitt TG, Lever AM, Dunnett SB, Rosser AE, Barker RA. Neural transplantation in Huntington's disease: the NEST-UK donor tissue microbiological screening program and review of the literature. Cell Transplant. 2006;15:279–94. [PubMed: 16898222]
• Fisher ER, Hayden MR. Multisource ascertainment of Huntington disease in Canada: prevalence and population at risk. Mov Disord. 2014;29:105–14. [PubMed: 24151181]
• Frank S, Testa CM, Stamler D, Kayson E, Davis C, Edmondson MC, Kinel S, Leavitt B, Oakes D, O'Neill C, et al. Effect of deutetrabenazine on chorea among patients with Huntington disease: a randomized clinical trial. JAMA. 2016;316:40–50. [PubMed: 27380342]
• Furtado S, Sossi V, Hauser RA, Samii A, Schulzer M, Murphy CB, Freeman TB, Stoessl AJ. Positron emission tomography after fetal transplantation in Huntington's disease. Ann Neurol. 2005;58:331–7. [PubMed: 16049929]
• Gaba AM, Zhang K, Marder K, Moskowitz CB, Werner P, Boozer CN. Energy balance in early-stage Huntington disease. Am J Clin Nutr. 2005;81:1335–41. [PubMed: 15941884]
• Gagnon KT, Pendergraff HM, Deleavey GF, Swayze EE, Potier P, Randolph J, Roesch EB, Chattopadhyaya J, Damha MJ, Bennett CF, Montaillier C, Lemaitre M, Corey DR. Allele-selective inhibition of mutant huntingtin expression with antisense oligonucleotides targeting the expanded CAG repeat. Biochemistry. 2010;49:10166–78. [PMC free article: PMC2991413] [PubMed: 21028906]
• Galvan L, André VM, Wang EA, Cepeda C, Levine MS. Functional differences between direct and indirect striatal output pathways in Huntington's disease. J Huntingtons Dis. 2012;1:17–25. [PMC free article: PMC4116084] [PubMed: 25063187]
• Gambardella A, Muglia M, Labate A, Magariello A, Gabriele AL, Mazzei R, Pirritano D, Conforti FL, Patitucci A, Valentino P, Zappia M, Quattrone A. Juvenile Huntington's disease presenting as progressive myoclonic epilepsy. Neurology. 2001;57:708–11. [PubMed: 11524486]
• GeM-HD Consortium. CAG repeat not polyglutamine length determines timing of Huntington's disease onset. Cell. 2019;178:887–900.e14. [PMC free article: PMC6700281] [PubMed: 31398342]
• GeM-HD Consortium. Identification of genetic factors that modify clinical onset of Huntington's disease. Cell. 2015;162:516–26. [PMC free article: PMC4524551] [PubMed: 26232222]
• Golding CV, Danchaivijitr C, Hodgson TL, Tabrizi SJ, Kennard C. Identification of an oculomotor biomarker of preclinical Huntington disease. Neurology. 2006;67:485–7. [PubMed: 16625001]
• Gonzalez-Alegre P, Afifi AK. Clinical characteristics of childhood-onset (juvenile) Huntington disease: report of 12 patients and review of the literature. J Child Neurol. 2006;21:223–9. [PubMed: 16901424]
• Goodman AO, Barker RA. How vital is sleep in Huntington's disease? J Neurol. 2010;257:882–97. [PubMed: 20333394]
• Graham RK, Slow EJ, Deng Y, Bissada N, Lu G, Pearson J, Shehadeh J, Leavitt BR, Raymond LA, Hayden MR. Levels of mutant huntingtin influence the phenotypic severity of Huntington disease in YAC128 mouse models. Neurobiol Dis. 2006;21:444–55. [PubMed: 16230019]
• Guo Z, Rudow G, Pletnikova O, Codispoti KE, Orr BA, Crain BJ, Duan W, Margolis RL, Rosenblatt A, Ross CA, Troncoso JC. Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease. Mov Disord. 2012;27:1379–86. [PMC free article: PMC3455126] [PubMed: 22975850]
• Gusella JF, Macdonald ME. Huntington's disease: the case for genetic modifiers. Genome Med. 2009;1:80. [PMC free article: PMC2768966] [PubMed: 19725930]
• Hadzi TC, Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Gillis T, Mysore JS, Gusella JF, MacDonald ME, Myers RH, Vonsattel JP. Assessment of cortical and striatal involvement in 523 Huntington disease brains. Neurology. 2012;79:1708–15. [PMC free article: PMC3468776] [PubMed: 23035064]
• Heinsen H, Rüb U, Bauer M, Ulmar G, Bethke B, Schüler M, Böcker F, Eisenmenger W, Götz M, Korr H, Schmitz C. Nerve cell loss in the thalamic mediodorsal nucleus in Huntington's disease. Acta Neuropathol. 1999;97:613–22. [PubMed: 10378380]
• Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, Macdonald ME, Gusella JF, Myers RH. Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG). Am J Med Genet A. 2009;149A:1375–81. [PMC free article: PMC2724761] [PubMed: 19507258]
• Hersch SM, Schifitto G, Oakes D, Bredlau AL, Meyers CM, Nahin R, Rosas HD, et al. The CREST-E study of creatine for Huntington disease: a randomized controlled trial. Neurology. 2017;89:594–601. [PMC free article: PMC5562960] [PubMed: 28701493]
• Ho AK, Robbins AO, Barker RA. Huntington's disease patients have selective problems with insight. Mov Disord. 2006;21:385–9. [PubMed: 16211608]
• Hu J, Liu J, Corey DR. Allele-selective inhibition of huntingtin expression by switching to an miRNA-like RNAi mechanism. Chem Biol. 2010;17:1183–8. [PMC free article: PMC3021381] [PubMed: 21095568]
• Huntington Study Group. Tetrabenazine as antichorea therapy in Huntington disease: a randomized controlled trial. Neurology. 2006;66:366–72. [PubMed: 16476934]
• Huntington Study Group. Unified Huntington's Disease Rating Scale: reliability and consistency. Mov Disord. 1996;11:136–42. [PubMed: 8684382]
• Huntington Study Group DOMINO Investigators. A futility study of minocycline in Huntington's disease. Mov Disord. 2010;25:2219–24. [PMC free article: PMC8801051] [PubMed: 20721920]
• Huntington Study Group PHAROS Investigators. At risk for Huntington disease: the PHAROS (Prospective Huntington At Risk Observational Study) cohort enrolled. Arch Neurol. 2006;63:991–6. [PubMed: 16831969]
• Jama M, Millson A, Miller CE, Lyon E. Triplet repeat primed PCR simplifies testing for Huntington disease. J Mol Diagn. 2013;15:255–62. [PubMed: 23414820]
• Jasper MJ, Hu DG, Liebelt J, Sherrin D, Watson R, Tremellen KP, Hussey ND. Singleton births after routine preimplantation genetic diagnosis using exclusion testing (D4S43 and D4S126) for Huntington's disease. Fertil Steril. 2006;85:597–602. [PubMed: 16500325]
• Johnson EB, Byrne LM, Gregory S, Rodrigues FB, Blennow K, Durr A, Leavitt BR, Roos RA, Zetterberg H, Tabrizi SJ, Scahill RI, Wild EJ, et al. Neurofilament light protein in blood predicts regional atrophy in Huntington disease. Neurology. 2018;90:e717–23. [PMC free article: PMC5818166] [PubMed: 29367444]
• Kalliolia E, Silajdžić E, Nambron R, Hill NR, Doshi A, Frost C, Watt H, Hindmarsh P, Björkqvist M, Warner TT. Plasma melatonin is reduced in Huntington's disease. Mov Disord. 2014;29:1511–5. [PubMed: 25164424]
• Kay C, Collins JA, Miedzybrodzka Z, Madore SJ, Gordon ES, Gerry N, Davidson M, Slama RA, Hayden MR. Huntington disease reduced penetrance alleles occur at high frequency in the general population. Neurology. 2016;87:282–8. [PMC free article: PMC4955276] [PubMed: 27335115]
• Kay C, Collins JA, Skotte NH, Southwell AL, Warby SC, Caron NS, Doty CN, Nguyen B, Griguoli A, Ross CJ, Squitieri F, Hayden MR. Huntingtin haplotypes provide prioritized target panels for allele-specific silencing in Huntington disease patients of European ancestry. Mol Ther. 2015;23:1759–71. [PMC free article: PMC4817952] [PubMed: 26201449]
• Kay C, Collins JA, Wright GEB, Baine F, Miedzybrodzka Z, Aminkeng F, Semaka AJ, McDonald C, Davidson M, Madore SJ, Gordon ES, Gerry NP, Cornejo-Olivas M, Squitieri F, Tishkoff S, Greenberg JL, Krause A, Hayden MR. The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population. Am J Med Genet B Neuropsychiatr Genet. 2018;177:346–57. [PubMed: 29460498]
• Keum JW, Shin A, Gillis T, Mysore JS, Abu Elneel K, Lucente D, Hadzi T, Holmans P, Jones L, Orth M, Kwak S, MacDonald ME, Gusella JF, Lee JM. The HTT CAG-expansion mutation determines age at death but not disease duration in Huntington disease. Am J Hum Genet. 2016;98:287–98. [PMC free article: PMC4746370] [PubMed: 26849111]
• Killoran A, Biglan KM. Current therapeutic options for Huntington's disease: good clinical practice versus evidence-based approaches? Mov Disord. 2014;29:1404–13. [PubMed: 25164707]
• Killoran A, Biglan KM, Jankovic J, Eberly S, Kayson E, Oakes D, et al. Characterization of the Huntington intermediate CAG repeat expansion phenotype in PHAROS. Neurology. 2013;80:2022–7. [PMC free article: PMC3716408] [PubMed: 23624566]
• Kim EH, Thu DC, Tippett LJ, Oorschot DE, Hogg VM, Roxburgh R, Synek BJ, Waldvogel HJ, Faull RL. Cortical interneuron loss and symptom heterogeneity in Huntington disease. Ann Neurol. 2014;75:717–27. [PubMed: 24771513]
• Kordasiewicz HB, Stanek LM, Wancewicz EV, Mazur C, McAlonis MM, Pytel KA, Artates JW, Weiss A, Cheng SH, Shihabuddin LS, Hung G, Bennett CF, Cleveland DW. Sustained therapeutic reversal of Huntington's disease by transient repression of huntingtin synthesis. Neuron. 2012;74:1031–44. [PMC free article: PMC3383626] [PubMed: 22726834]
• Kuemmerle S, Gutekunst CA, Klein AM, Li XJ, Li SH, Beal MF, Hersch SM, Ferrante RJ. Huntington aggregates may not predict neuronal death in Huntington's disease. Ann Neurol. 1999;46:842–9. [PubMed: 10589536]
• Langbehn DR, Brinkman RR, Falush D, Paulsen JS, Hayden MR, et al. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length. Clin Genet. 2004;65:267–77. [PubMed: 15025718]
• Langbehn DR, Hayden MR, Paulsen JS, et al. CAG-repeat length and the age of onset in Huntington disease (HD): a review and validation study of statistical approaches. Am J Med Genet B Neuropsychiatr Genet. 2010;153B:397–408. [PMC free article: PMC3048807] [PubMed: 19548255]
• Laplanche JL, Hachimi KH, Durieux I, Thuillet P, Defebvre L, Delasnerie-Laupretre N, Peoc'h K, Foncin JF, Destee A. Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene. Brain. 1999;122:2375–86. [PubMed: 10581230]
• Larsson MU, Luszcz MA, Bui TH, Wahlin TB. Depression and suicidal ideation after predictive testing for Huntington's disease: a two-year follow-up study. J Genet Couns. 2006;15:361–74. [PubMed: 16967331]
• Lee JM, Ramos EM, Lee JH, Gillis T, Mysore JS, Hayden MR, Warby SC, Morrison P, Nance M, Ross CA, Margolis RL, Squitieri F, Orobello S, Di Donato S, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Abramson RK, Marder K, Sequeiros J, Paulsen JS, Landwehrmeyer GB, Myers RH, MacDonald ME, Gusella JF, et al. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012;78:690–5. [PMC free article: PMC3306163] [PubMed: 22323755]
• Levin BC, Richie KL, Jakupciak JP. Advances in Huntington's disease diagnostics: development of a standard reference material. Expert Rev Mol Diagn. 2006;6:587–96. [PubMed: 16824032]
• Li JL, Hayden MR, Warby SC, Durr A, Morrison PJ, Nance M, Ross CA, Margolis RL, Rosenblatt A, Squitieri F, Frati L, Gomez-Tortosa E, Garcia CA, Suchowersky O, Klimek ML, Trent RJ, McCusker E, Novelletto A, Frontali M, Paulsen JS, Jones R, Ashizawa T, Lazzarini A, Wheeler VC, Prakash R, Xu G, Djoussé L, Mysore JS, Gillis T, Hakky M, Cupples LA, Saint-Hilaire MH, Cha JH, Hersch SM, Penney JB, Harrison MB, Perlman SL, Zanko A, Abramson RK, Lechich AJ, Duckett A, Marder K, Conneally PM, Gusella JF, MacDonald ME, Myers RH. Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study. BMC Med Genet. 2006;7:71. [PMC free article: PMC1586197] [PubMed: 16914060]
• Liu D, Long JD, Zhang Y, Raymond LA, Marder K, Rosser A, McCusker EA, Mills JA, Paulsen JS, et al. Motor onset and diagnosis in Huntington disease using the diagnostic confidence level. J Neurol. 2015;262:2691–8. [PMC free article: PMC4666501] [PubMed: 26410751]
• Lopez WO, Nikkhah G, Schültke E, Furlanetti L, Trippel M. Stereotactic planning software for human neurotransplantation: suitability in 22 surgical cases of Huntington's disease. Restor Neurol Neurosci. 2014;32:259–68. [PubMed: 24164802]
• MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA. Recommendations for the predictive genetic test in Huntington's disease. Clin Genet. 2013;83:221–31. [PubMed: 22642570]
• Majid DS, Aron AR, Thompson W, Sheldon S, Hamza S, Stoffers D, Holland D, Goldstein J, Corey-Bloom J, Dale AM. Basal ganglia atrophy in prodromal Huntington's disease is detectable over one year using automated segmentation. Mov Disord. 2011;26:2544–51. [PMC free article: PMC5615846] [PubMed: 21932302]
• Marshall J, White K, Weaver M, Flury Wetherill L, Hui S, Stout JC, Johnson SA, Beristain X, Gray J, Wojcieszek J, Foroud T. Specific psychiatric manifestations among preclinical Huntington disease mutation carriers. Arch Neurol. 2007;64:116–21. [PubMed: 17210818]
• Martino D, Stamelou M, Bhatia KP. The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician. J Neurol Neurosurg Psychiatry. 2013;84:650–6. [PMC free article: PMC3646286] [PubMed: 22993450]
• McBride JL, Pitzer MR, Boudreau RL, Dufour B, Hobbs T, Ojeda SR, Davidson BL. Preclinical safety of RNAi-mediated HTT suppression in the rhesus macaque as a potential therapy for Huntington's disease. Mol Ther. 2011;19:2152–62. [PMC free article: PMC3242667] [PubMed: 22031240]
• McGarry A, McDermott M, Kieburtz K, de Blieck EA, Beal F, Marder K, Ross C, Shoulson I, Gilbert P, Mallonee WM, Guttman M, Wojcieszek J, Kumar R, LeDoux MS, Jenkins M, Rosas HD, Nance M, Biglan K, Como P, Dubinsky RM, Shannon KM, O'Suilleabhain P, Chou K, Walker F, Martin W, Wheelock VL, McCusker E, Jankovic J, Singer C, Sanchez-Ramos J, Scott B, Suchowersky O, Factor SA, Higgins DS Jr, Molho E, Revilla F, Caviness JN, Friedman JH, Perlmutter JS, Feigin A, Anderson K, Rodriguez R, McFarland NR, Margolis RL, Farbman ES, Raymond LA, Suski V, Kostyk S, Colcher A, Seeberger L, Epping E, Esmail S, Diaz N, Fung WL, Diamond A, Frank S, Hanna P, Hermanowicz N, Dure LS, Cudkowicz M, et al. A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease. Neurology. 2017;88:152–9. [PMC free article: PMC5224719] [PubMed: 27913695]
• Mehrabi NF, Waldvogel HJ, Tippett LJ, Hogg VM, Synek BJ, Faull RL. Symptom heterogeneity in Huntington's disease correlates with neuronal degeneration in the cerebral cortex. Neurobiol Dis. 2016;96:67–74. [PubMed: 27569581]
• Mestre T, Ferreira J, Coelho MM, Rosa M, Sampaio C. Therapeutic interventions for symptomatic treatment in Huntington's disease. Cochrane Database Syst Rev. 2009;3:CD006456. [PubMed: 19588393]
• Michalik A, Van Broeckhoven C. Pathogenesis of polyglutamine disorders: aggregation revisited. Hum Mol Genet. 2003;12(Spec No 2):R173–86. [PubMed: 14504263]
• Montoya A, Price BH, Menear M, Lepage M. Brain imaging and cognitive dysfunctions in Huntington's disease. J Psychiatry Neurosci. 2006;31:21–9. [PMC free article: PMC1325063] [PubMed: 16496032]
• Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edstrom L, Anvret M, Prusiner SB. Huntington disease phenocopy is a familial prion disease. Am J Hum Genet. 2001;69:1385–8. [PMC free article: PMC1235549] [PubMed: 11593450]
• Morton AJ. Circadian and sleep disorder in Huntington's disease. Exp Neurol. 2013;243:34–44. [PubMed: 23099415]
• Moss DJH, Pardiñas AF, Langbehn D, Lo K, Leavitt BR, Roos R, Durr A, Mead S, Holmans P, Jones L, Tabrizi SJ, et al. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. Lancet Neurol. 2017;16:701–11. [PubMed: 28642124]
• Moutou C, Gardes N, Viville S. New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications. Eur J Hum Genet. 2004;12:1007–14. [PubMed: 15470361]
• Nahhas FA, Garbern J, Krajewski KM, Roa BB, Feldman GL. Juvenile onset Huntington disease resulting from a very large maternal expansion. Am J Med Genet A. 2005;137A:328–31. [PubMed: 16096998]
• Nance MA, Myers RH. Juvenile onset Huntington's disease--clinical and research perspectives. Ment Retard Dev Disabil Res Rev. 2001;7:153–7. [PubMed: 11553930]
• Okamoto S, Pouladi MA, Talantova M, Yao D, Xia P, Ehrnhoefer D.E, Zaidi R, Clemente A, Kaul M, Graham RK, Zhang D, Chen HS, Tong G, Hayden MR, Lipton SA. Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingin. Nat Med. 2009;15:1407–13. [PMC free article: PMC2789858] [PubMed: 19915593]
• Ondo WG, Mejia NI, Hunter CB. A pilot study of the clinical efficacy and safety of memantine for Huntington's disease. Parkinsonism Relat Disord. 2007;13:453–4. [PubMed: 17046312]
• Paulsen JS. Functional imaging in Huntington's disease. Exp Neurol. 2009;216:272–7. [PMC free article: PMC3810959] [PubMed: 19171138]
• Paulsen JS, Hayden M, Stout JC, Langbehn DR, Aylward E, Ross CA, Guttman M, Nance M, Kieburtz K, Oakes D, Shoulson I, Kayson E, Johnson S, Penziner E. Preparing for preventive clinical trials: the Predict-HD study. Arch Neurol. 2006;63:883–90. [PubMed: 16769871]
• Paulsen JS, Hoth KF, Nehl C, Stierman L. Critical periods of suicide risk in Huntington's disease. Am J Psychiatry. 2005a;162:725–31. [PubMed: 15800145]
• Paulsen JS, Langbehn DR, Stout JC, Aylward E, Ross CA, Nance M, Guttman M, Johnson S, MacDonald M, Beglinger LJ, Duff K, Kayson E, Biglan K, Shoulson I, Oakes D, Hayden M, et al. Detection of Huntington's disease decades before diagnosis: the Predict-HD study. J Neurol Neurosurg Psychiatry. 2008;79:874–80. [PMC free article: PMC2569211] [PubMed: 18096682]
• Paulsen JS, Nehl C, Hoth KF, Kanz JE, Benjamin M, Conybeare R, McDowell B, Turner B. Depression and stages of Huntington's disease. J Neuropsychiatry Clin Neurosci. 2005b;17:496–502. [PubMed: 16387989]
• Peinemann A, Schuller S, Pohl C, Jahn T, Weindl A, Kassubek J. Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: a neuropsychological and voxel-based morphometric study. J Neurol Sci. 2005;239:11–9. [PubMed: 16185716]
• Petersén A, Björkqvist M. Hypothalamic-endocrine aspects in Huntington's disease. Eur J Neurosci. 2006;24:961–7. [PubMed: 16925587]
• Petersén A, Gil J, Maat-Schieman ML, Björkqvist M, Tanila H, Araújo IM, Smith R, Popovic N, Wierup N, Norlén P, Li JY, Roos RA, Sundler F, Mulder H, Brundin P. Orexin loss in Huntington's disease. Hum Mol Genet. 2005;14:39–47. [PubMed: 15525658]
• Pfister EL, DiNardo N, Mondo E, Borel F, Conroy F, Fraser C, Gernoux G, Han X, Hu D, Johnson E, Kennington L, Liu P, Reid SJ, Sapp E, Vodicka P, Kuchel T, Morton AJ, Howland D, Moser R, Sena-Esteves M, Gao G, Mueller C, DiFiglia M, Aronin N. Artificial miRNAs reduce human mutant huntingtin throughout the striatum in a transgenic sheep model of Huntington's disease. Hum Gene Ther. 2018;29:663–73. [PMC free article: PMC6909722] [PubMed: 29207890]
• Pfister EL, Zamore PD. Huntington's disease: silencing a brutal killer. Exp Neurol. 2009;220:226–9. [PMC free article: PMC2805437] [PubMed: 19786020]
• Phillips W, Shannon KM, Barker RA. The current clinical management of Huntington's disease. Mov Disord. 2008;23:1491–504. [PubMed: 18581443]
• Potter NT, Spector EB, Prior TW. Technical standards and guidelines for Huntington disease testing. Genet Med. 2004;6:61–5. [PubMed: 14726813]
• Pouladi MA, Graham RK, Karasinska JM, Xie Y, Santos RD, Petersén A, Hayden MR. Prevention of depressive behaviour in the YAC128 mouse model of Huntington disease by mutation at residue 586 of huntingtin. Brain. 2009;132:919–32. [PubMed: 19224899]
• Pratley RE, Salbe AD, Ravussin E, Caviness JN. Higher sedentary energy expenditure in patients with Huntington's disease. Ann Neurol. 2000;47:64–70. [PubMed: 10632102]
• Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis. Mov Disord. 2012;27:1083–91. [PubMed: 22692795]
• Puri BK, Leavitt BR, Hayden MR, Ross CA, Rosenblatt A, Greenamyre JT, Hersch S, Vaddadi KS, Sword A, Horrobin DF, Manku M, Murck H. Ethyl-EPA in Huntington disease: a double-blind, randomized, placebo-controlled trial. Neurology. 2005;65:286–92. [PubMed: 16043801]
• Quarrell OW, Nance MA, Nopoulos P, Paulsen JS, Smith JA, Squitieri F. Managing juvenile Huntington's disease. Neurodegener Dis Manag. 2013:3. [PMC free article: PMC3883192] [PubMed: 24416077]
• Ravina B, Romer M, Constantinescu R, Biglan K, Brocht A, Kieburtz K, Shoulson I, McDermott MP. The relationship between CAG repeat length and clinical progression in Huntington's disease. Mov Disord. 2008;23:1223–7. [PubMed: 18512767]
• Rawlins MD, Wexler NS, Wexler AR, Tabrizi SJ, Douglas I, Evans SJ, Smeeth L. The prevalence of Huntington's disease. Neuroepidemiology. 2016;46:144–53. [PubMed: 26824438]
• Rego AC, de Almeida LP. Molecular targets and therapeutic strategies in Huntington's disease. Curr Drug Targets CNS Neurol Disord. 2005;4:361–81. [PubMed: 16101555]
• Reilmann R. Deutetrabenazine-not a revolution but welcome evolution for treating chorea in Huntington disease. JAMA Neurol. 2016;73:1404–6. [PubMed: 27749952]
• Reilmann R, Leavitt BR, Ross CA. Diagnostic criteria for Huntington's disease based on natural history. Mov Disord. 2014;29:1335–41. [PubMed: 25164527]
• Robbins AO, Ho AK, Barker RA. Weight changes in Huntington's disease. Eur J Neurol. 2006;13:e7. [PubMed: 16879284]
• Robins Wahlin TB. To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease. Patient Educ Couns. 2007;65:279–87. [PubMed: 17000074]
• Robins Wahlin TB, Backman L, Lundin A, Haegermark A, Winblad B, Anvret M. High suicidal ideation in persons testing for Huntington's disease. Acta Neurol Scand. 2000;102:150–61. [PubMed: 10987374]
• Rosenblatt A. Neuropsychiatry of Huntington's disease. Dialogues Clin Neurosci. 2007;9:191–7. [PMC free article: PMC3181855] [PubMed: 17726917]
• Ross CA, Aylward EH, Wild EJ, Langbehn DR, Long JD, Warner JH, Scahill RI, Leavitt BR, Stout JC, Paulsen JS, Reilmann R, Unschuld PG, Wexler A, Margolis RL, Tabrizi SJ. Huntington disease: natural history, biomarkers and prospects for therapeutics. Nat Rev Neurol. 2014;10:204–16. [PubMed: 24614516]
• Rupp J, Blekher T, Jackson J, Beristain X, Marshall J, Hui S, Wojcieszek J, Foroud T. Progression in prediagnostic Huntington disease. J Neurol Neurosurg Psychiatry. 2010;81:379–84. [PMC free article: PMC2872788] [PubMed: 19726414]
• Saft C, Lauter T, Kraus PH, Przuntek H, Andrich JE. Dose-dependent improvement of myoclonic hyperkinesia due to Valproic acid in eight Huntington's disease patients: a case series. BMC Neurol. 2006;6:11. [PMC free article: PMC1413552] [PubMed: 16507108]
• Saudou F, Humbert S. The Biology of Huntingtin. Neuron. 2016 2016 Mar 2;89(5):910–26. [PubMed: 26938440]
• Scahill RI, Wild EJ, Tabrizi SJ. Biomarkers for Huntington's disease: an update. Expert Opin Med Diagn. 2012;6:371–5. [PubMed: 23480802]
• Schneider SA, Walker RH, Bhatia KP. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test. Nat Clin Pract Neurol. 2007;3:517–25. [PubMed: 17805246]
• Semaka A, Creighton S, Warby S, Hayden MR. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles. Clin Genet. 2006;70:283–94. [PubMed: 16965319]
• Semaka A, Hayden MR. Evidence-based genetic counselling implications for Huntington disease intermediate allele predictive test results. Clin Genet. 2014;85:303–11. [PubMed: 24256063]
• Semaka A, Kay C, Belfroid RD, Bijlsma EK, Losekoot M, van Langen IM, van Maarle MC, Oosterloo M, Hayden MR, van Belzen MJ. A new mutation for Huntington disease following maternal transmission of an intermediate allele. Eur J Med Genet. 2015;58:28–30. [PubMed: 25464109]
• Semaka A, Kay C, Doty C, Collins JA, Bijlsma EK, Richards F, Goldberg YP, Hayden MR. CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease. J Med Genet. 2013a;50:696–703. [PubMed: 23896435]
• Semaka A, Kay C, Doty CN, Collins JA, Tam N, Hayden MR. High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general population. Am J Med Genet B Neuropsychiatr Genet. 2013b;162B:864–71. [PubMed: 24038799]
• Sermon K, De Rijcke M, Lissens W, De Vos A, Platteau P, Bonduelle M, Devroey P, Van Steirteghem A, Liebaers I. Preimplantation genetic diagnosis for Huntington's disease with exclusion testing. Eur J Hum Genet. 2002;10:591–8. [PubMed: 12357329]
• Siesling S, van Vugt JP, Zwinderman KA, Kieburtz K, Roos RA. Unified Huntington's disease rating scale: a follow up. Mov Disord. 1998;13:915–9. [PubMed: 9827615]
• Singh-Bains MK, Tippett LJ, Hogg VM, Synek BJ, Roxburgh RH, Waldvogel HJ, Faull RL. Globus pallidus degeneration and clinicopathological features of Huntington disease. Ann Neurol. 2016;80:185–201. [PubMed: 27255697]
• Sipilä JO, Hietala M, Siitonen A, Päivärinta M, Majamaa K. Epidemiology of Huntington's disease in Finland. Parkinsonism Relat Disord. 2015;21:46–9. [PubMed: 25466405]
• Skirton H. Huntington disease: a nursing perspective. Medsurg Nurs. 2005;14:167–72. [PubMed: 16035633]
• Skotte NH, Southwell AL, Østergaard ME, Carroll JB, Warby SC, Doty CN, Petoukhov E, Vaid K, Kordasiewicz H, Watt AT, Freier SM, Hung G, Seth PP, Bennett CF, Swayze EE, Hayden MR. Allele-specific suppression of mutant huntingtin using antisense oligonucleotides: providing a therapeutic option for all Huntington disease patients. PLoS One. 2014;9:e107434. [PMC free article: PMC4160241] [PubMed: 25207939]
• Slaughter JR, Martens MP, Slaughter KA. Depression and Huntington's disease: prevalence, clinical manifestations, etiology, and treatment. CNS Spectr. 2001;6:306–26. [PubMed: 16113629]
• Slow EJ, Graham RK, Hayden MR. To be or not to be toxic: aggregations in Huntington and Alzheimer disease. Trends Genet. 2006;22:408–11. [PubMed: 16806565]
• Slow EJ, Graham RK, Osmand AP, Devon RS, Lu G, Deng Y, Pearson J, Vaid K, Bissada N, Wetzel R, Leavitt BR, Hayden MR. Absence of behavioral abnormalities and neurodegeneration in vivo despite widespread neuronal huntingtin inclusions. Proc Natl Acad Sci U S A. 2005;102:11402–7. [PMC free article: PMC1183566] [PubMed: 16076956]
• Southwell AL, Kordasiewicz HB, Langbehn D, Skotte NH, Parsons MP, Villanueva EB, Caron NS, Østergaard ME, Anderson LM, Xie Y, Cengio LD, Findlay-Black H, Doty CN, Fitsimmons B, Swayze EE, Seth PP, Raymond LA, Frank Bennett C, Hayden MR. Huntingtin suppression restores cognitive function in a mouse model of Huntington's disease. Sci Transl Med. 2018;10:eaar3959. [PubMed: 30282695]
• Southwell AL, Skotte NH, Kordasiewicz HB, Ostergaard ME, Watt AT, Carroll JB, Doty CN, Villanueva EB, Petoukhov E, Vaid K, Xie Y, Freier SM, Swayze EE, Seth PP, Bennett CF, Hayden MR. In vivo evaluation of candidate allele-specific mutant huntingtin gene silencing antisense oligonucleotides. Mol Ther. 2014;22:2093–106. [PMC free article: PMC4429695] [PubMed: 25101598]
• Southwell AL, Smith SE, Davis TR, Caron NS, Villanueva EB, Xie Y, Collins JA, Ye ML, Sturrock A, Leavitt BR, Schrum AG, Hayden MR. Ultrasensitive measurement of huntingtin protein in cerebrospinal fluid demonstrates increase with Huntington disease stage and decrease following brain huntingtin suppression. Sci Rep. 2015;5:12166. [PMC free article: PMC4502413] [PubMed: 26174131]
• Squitieri F, Frati L, Ciarmiello A, Lastoria S, Quarrell O. Juvenile Huntington's disease: does a dosage-effect pathogenic mechanism differ from the classical adult disease? Mech Ageing Dev. 2006;127:208–12. [PubMed: 16274727]
• Squitieri F, Maglione V, Orobello S, Fornai F. Genotype-, aging-dependent abnormal caspase activity in Huntington disease blood cells. J Neural Transm. 2011;118:1599–607. [PubMed: 21519949]
• Stamler D, Bradbury M, Brown F. The pharmacokinetics and safety of deuterated-tetrabenazine. Neurology. 2013;80 Suppl:210.
• Stanek LM, Sardi SP, Mastis B, Richards AR, Treleaven CM, Taksir T, Misra K, Cheng SH, Shihabuddin LS. Silencing mutant huntingtin by adeno-associated virus-mediated RNA interference ameliorates disease manifestations in the YAC128 mouse model of Huntington's disease. Hum Gene Ther. 2014;25:461–74. [PMC free article: PMC4028091] [PubMed: 24484067]
• Stern HJ, Harton GL, Sisson ME, Jones SL, Fallon LA, Thorsell LP, Getlinger ME, Black SH, Schulman JD. Non-disclosing preimplantation genetic diagnosis for Huntington disease. Prenat Diagn. 2002;22:503–7. [PubMed: 12116316]
• Stoy N, McKay E. Weight loss in Huntington's disease. Ann Neurol. 2000;48:130–1. [PubMed: 10894233]
• Tabrizi SJ, Langbehn DR, Leavitt BR, Roos RA, Durr A, Craufurd D, Kennard C, Hicks SL, Fox NC, Scahill RI, Borowsky B, Tobin AJ, Rosas HD, Johnson H, Reilmann R, Landwehrmeyer B, Stout JC, et al. Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data. Lancet Neurol. 2009;8:791–801. [PMC free article: PMC3725974] [PubMed: 19646924]
• Tabrizi SJ, Leavitt BR, Landwehrmeyer GB, Wild EJ, Saft C, Barker RA, Blair NF, Craufurd D, Priller J, Rickards H, Rosser A, Kordasiewicz HB, Czech C, Swayze EE, Norris DA, Baumann T, Gerlach I, Schobel SA, Paz E, Smith AV, Bennett CF, Lane RM, et al. Targeting Huntingtin expression in patients with Huntington's disease. N Engl J Med. 2019;380:2307–16. [PubMed: 31059641]
• Tabrizi SJ, Reilmann R, Roos RA, Durr A, Leavitt B, Owen G, Jones R, Johnson H, Craufurd D, Hicks SL, Kennard C, Landwehrmeyer B, Stout JC, Borowsky B, Scahill RI, Frost C, Langbehn DR, et al. Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data. Lancet Neurol. 2012;11:42–53. [PubMed: 22137354]
• Tabrizi SJ, Scahill RI, Durr A, Roos RA, Leavitt BR, Jones R, Landwehrmeyer GB, Fox NC, Johnson H, Hicks SL, Kennard C, Craufurd D, Frost C, Langbehn DR, Reilmann R, Stout JC, et al. Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis. Lancet Neurol. 2011;10:31–42. [PubMed: 21130037]
• Tabrizi SJ, Scahill RI, Owen G, Durr A, Leavitt BR, Roos RA, Borowsky B, Landwehrmeyer B, Frost C, Johnson H, Craufurd D, Reilmann R, Stout JC, Langbehn DR, et al. Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data. Lancet Neurol. 2013;12:637–49. [PubMed: 23664844]
• Taylor S. Gender differences in attitudes among those at risk for Huntington's disease. Genet Test. 2005;9:152–7. [PubMed: 15943556]
• Telenius H, Kremer B, Goldberg YP, Theilmann J, Andrew SE, Zeisler J, Adam S, Greenberg C, Ives EJ, Clarke LA, et al. Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm. Nat Genet. 1994;6:409–14. [PubMed: 8054984]
• Thu DC, Oorschot DE, Tippett LJ, Nana AL, Hogg VM, Synek BJ, Luthi-Carter R, Waldvogel HJ, Faull RL. Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease. Brain. 2010;133(Pt 4):1094–110. [PubMed: 20375136]
• Timman R, Claus H, Slingerland H, van der Schalk M, Demeulenaere S, Roos RA, Tibben A. Nature and development of Huntington disease in a nursing home population: The Behavior Observation Scale Huntington (BOSH). Cogn Behav Neurol. 2005;18:215–22. [PubMed: 16340395]
• Trejo A, Tarrats RM, Alonso ME, Boll MC, Ochoa A, Velásquez L. Assessment of the nutrition status of patients with Huntington's disease. Nutrition. 2004;20:192–6. [PubMed: 14962685]
• Valenza M, Cattaneo E. Cholesterol dysfunction in neurodegenerative diseases: Is Huntington's disease in the list? Prog Neurobiol. 2006;80:165–76. [PubMed: 17067733]
• van der Burg JM, Björkqvist M, Brundin P. Beyond the brain: widespread pathology in Huntington's disease. Lancet Neurol. 2009;8:765–74. [PubMed: 19608102]
• van der Burg JMM, Gardiner SL, Ludolph AC, Landwehrmeyer GB, Roos RAC, Aziz NA. Body weight is a robust predictor of clinical progression in Huntington disease. Ann Neurol. 2017;82:479–83. [PubMed: 28779551]
• van Duijn E, Vrijmoeth EM, Giltay EJ, Bernhard Landwehrmeyer G, et al. Suicidal ideation and suicidal behavior according to the C-SSRS in a European cohort of Huntington's disease gene expansion carriers. J Affect Disord. 2018;228:194–204. [PubMed: 29253686]
• Videnovic A, Leurgans S, Fan W, Jaglin J, Shannon KM. Daytime somnolence and nocturnal sleep disturbances in Huntington disease. Parkinsonism Relat Disord. 2009;15:471–4. [PubMed: 19041273]
• Vonsattel JP, DiFiglia M. Huntington disease. J Neuropathol Exp Neurol. 1998;57:369–84. [PubMed: 9596408]
• Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Bird ED, Richardson EP Jr. Neuropathological classification of Huntington's disease. J Neuropathol Exp Neurol. 1985;44:559–77. [PubMed: 2932539]
• Waldvogel HJ, Kim EH, Tippett LJ, Vonsattel JP, Faull RL. The neuropathology of Huntington's disease. Curr Top Behav Neurosci. 2015;22:33–80. [PubMed: 25300927]
• Wang R, Ross CA, Cai H, Cong WN, Daimon CM, Carlson OD, Egan JM, Siddiqui S, Maudsley S, Martin B. Metabolic and hormonal signatures in pre-manifest and manifest Huntington's disease patients. Front Physiol. 2014;5:231. [PMC free article: PMC4066441] [PubMed: 25002850]
• Warby SC, Montpetit A, Hayden AR, Carroll JB, Butland SL, Visscher H, Collins JA, Semaka A, Hudson TJ, Hayden MR. CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup. Am J Hum Genet. 2009;84:351–66. [PMC free article: PMC2668007] [PubMed: 19249009]
• Warby SC, Visscher H, Collins JA, Doty CN, Carter C, Butland SL, Hayden AR, Kanazawa I, Ross CJ, Hayden MR. HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia. Eur J Hum Genet. 2011;19:561–6. [PMC free article: PMC3083615] [PubMed: 21248742]
• Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayan J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, Wiktorski S, Hodes ME, Conneally PM, Penney JB, Gusella J, Cha JH, Irizarry M, Rosas D, Hersch S, Hollingsworth Z, MacDonald M, Young AB, Andresen JM, Housman DE, De Young MM, Bonilla E, Stillings T, Negrette A, Snodgrass SR, Martinez-Jaurrieta MD, Ramos-Arroyo MA, Bickham J, Ramos JS, Marshall F, Shoulson I, Rey GJ, Feigin A, Arnheim N, Acevedo-Cruz A, Acosta L, Alvir J, Fischbeck K, Thompson LM, Young A, Dure L, O'Brien CJ, Paulsen J, Brickman A, Krch D, Peery S, Hogarth P, Higgins DS Jr, Landwehrmeyer B. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proc Natl Acad Sci U S A. 2004;101:3498–503. [PMC free article: PMC373491] [PubMed: 14993615]
• Wild EJ, Boggio R, Langbehn D, Robertson N, Haider S, Miller JR, Zetterberg H, Leavitt BR, Kuhn R, Tabrizi SJ, Macdonald D, Weiss A. Quantification of mutant huntingtin protein in cerebrospinal fluid from Huntington's disease patients. J Clin Invest. 2015;125:1979–86. [PMC free article: PMC4463213] [PubMed: 25844897]
• Wild EJ, Tabrizi SJ. Targets for future clinical trials in Huntington's disease: What's in the pipeline? Mov Disord. 2014;29:1434–45. [PMC free article: PMC4265300] [PubMed: 25155142]
• Williams JK, Skirton H, Paulsen JS, Tripp-Reimer T, Jarmon L, McGonigal Kenney M, Birrer E, Hennig BL, Honeyford J. The emotional experiences of family carers in Huntington disease. J Adv Nurs. 2009;65:789–98. [PMC free article: PMC3807601] [PubMed: 19228233]
• Wright GEB, Collins JA, Kay C, McDonald C, Dolzhenko E, Xia Q, Bečanović K, Drögemöller BI, Semaka A, Nguyen CM, Trost B, Richards F, Bijlsma EK, Squitieri F, Ross CJD, Scherer SW, Eberle MA, Yuen RKC, Hayden MR. Length of uninterrupted CAG, independent of polyglutamine size, results in increased somatic instability, hastening onset of Huntington disease. Am J Hum Genet. 2019;104:1116–26. [PMC free article: PMC6556907] [PubMed: 31104771]
• Xu M, Wu ZY. Huntington disease in Asia. Chin Med J (Engl). 2015;128:1815–9. [PMC free article: PMC4733723] [PubMed: 26112725]
• Yoon G, Kramer J, Zanko A, Guzijan M, Lin S, Foster-Barber A, Boxer AL. Speech and language delay are early manifestations of juvenile-onset Huntington disease. Neurology. 2006;67:1265–7. [PubMed: 17030763]
• Youssov K, Dolbeau G, Maison P, Boissé M-F, Cleret de Langavant L, Roos RAC, et al. Unified Huntington's disease rating scale for advanced patients: validation and follow-up study. Mov Disord. 2013;28:1717–23. [PMC free article: PMC5071381] [PubMed: 24166899]