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Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis

Synonym: POIKTMP

, MD, PhD, , DVM, PhD, and , MD, PhD.

Author Information and Affiliations

Initial Posting: ; Last Revision: September 9, 2021.

Estimated reading time: 17 minutes

Summary

Clinical characteristics.

Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) is characterized by the skin findings of poikiloderma (typically beginning in the first six months and mainly localized to the face), hypohidrosis with heat intolerance, mild lymphedema of the extremities, chronic erythematous and scaly skin lesions on the extremities, sclerosis of the digits, and mild palmoplantar keratoderma. Scalp hair, eyelashes, and/or eyebrows are typically sparse. Muscle contractures are usually seen in childhood and can be present as early as age two years. The majority of affected individuals develop progressive weakness of the proximal and distal muscles of all four limbs. Some adults develop progressive interstitial pulmonary fibrosis, which can be life threatening within three to four years after respiratory symptoms appear. Other features are exocrine pancreatic insufficiency, liver impairment, hematologic abnormalities, relative short stature, and cataract.

Diagnosis/testing.

The diagnosis of POIKTMP is established in a proband with early-onset poikiloderma with other findings, especially muscle contractures and/or muscle weakness and a heterozygous missense pathogenic variant in FAM111B identified by molecular genetic testing.

Management.

Treatment of manifestations: Dermatologic manifestations are treated with avoidance of excessive sun exposure and use of sunscreens with both UVA and UVB protection; avoidance of excessive heat exposure and control of fever, especially in early childhood; routine management of lymphedema; emollients, topical steroids for eczema-like lesions. For older individuals, pulsed dye laser may be an option for cosmesis of the telangiectatic component of the rash. Physical therapy and exercise to promote mobility and prevent contractures. Use of self-inflating manual-ventilation bag or mechanical insufflation-exsufflation device if needed for lung disease; noninvasive ventilation if needed. Pancreatic enzyme supplementation for pancreatic exocrine insufficiency.

Surveillance: Annual surveillance (or frequency as needed) includes dermatologic examination, physical therapy assessment for muscle weakness and/or contractures, assessment for orthopedic complications (contractures, especially of the Achilles tendon, and scoliosis), pulmonary function testing, serum transaminases (SGOT, SGPT), alkaline phosphatase, gamma-glutamyl transferase, blood ionogram including calcium, TSH, complete blood count with differential), and ophthalmologic examination.

Agents/circumstances to avoid: Excessive sun exposure (may exacerbate the rash), exposure to heat because of heat intolerance.

Genetic counseling.

POIKTMP is inherited in an autosomal dominant manner. In approximately 50% of affected individuals, the FAM111B pathogenic variant is inherited and in approximately 50% it is de novo. Each child of an individual with POIKTMP has a 50% chance of inheriting the FAM111B pathogenic variant. Once the FAM111B pathogenic variant has been identified in an affected family member, prenatal and preimplantation genetic testing are possible.

Diagnosis

Suggestive Findings

Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) should be suspected in individuals with the following clinical and imaging findings.

Clinical findings

  • Skin (Figure 1 and Figure 2):
    • Early-onset poikiloderma (characterized by erythema of the cheeks and face, skin atrophy, telangiectasias, and mottled pigmentation)
    • Hypotrichosis with sparse scalp hair, sparse or absent eyelashes and/or eyebrows
    • Hypohidrosis with heat intolerance
    • Mild lymphedema of the extremities
  • Multiple contractures, in particular triceps surae contractures in childhood
  • Myopathy with diffuse progressive muscular weakness, scoliosis
  • Restrictive pulmonary syndrome and/or pulmonary fibrosis
  • Exocrine pancreatic insufficiency
  • Liver impairment
  • Hematologic abnormalities (e.g., eosinophilia, thrombocytopenia, and/or bone marrow hypocellularity)
  • Other
    • Relative short stature
    • Cataract
    • Nail dystrophy
Figure 1.

Figure 1.

Facial and scalp skin lesions A-E. Poikiloderma and alopecia of the scalp, eyebrows, and eyelashes in childhood

Figure 2.

Figure 2.

Skin lesions of the upper and lower limbs A. Eczema-like and psoriasis-like dermatosis of the upper limbs

Imaging findings

  • See Figure 3. Muscle MRI typically shows severe diffuse fatty infiltration of the legs, especially:
    • The vastus lateralis muscles (with relative sparing of the tibialis posterior); and
    • The anterior compartment of thighs (with relative sparing of posterior compartment).
  • These findings can confirm muscle involvement in asymptomatic individuals.
Figure 3.

Figure 3.

Muscle MRI (coronal images of the thighs and calves; T1-weighted sequence) A. Diffuse bright appearance of the anterior compartment of the thighs (upper images), particularly in the vastus lateralis muscles, and the posterior compartment of the calves (more...)

Establishing the Diagnosis

The diagnosis of POIKTMP is established in a proband with early-onset poikiloderma with other findings (especially muscle contractures and/or muscle weakness) and a heterozygous pathogenic missense variant in FAM111B identified on molecular genetic testing (Table 1).

Molecular genetic testing approaches can include a combination of gene-targeted testing (single-gene testing, multigene panel) and comprehensive genomic testing (exome sequencing, genome sequencing) depending on the phenotype.

Gene-targeted testing requires that the clinician determine which gene(s) are likely involved, whereas genomic testing does not. Individuals with the distinctive findings described in Suggestive Findings are likely to be diagnosed using gene-targeted testing (see Option 1), whereas those in whom the diagnosis of POIKTMP has not been considered are more likely to be diagnosed using genomic testing (see Option 2).

Option 1

Single-gene testing. Sequence analysis of FAM111B to detect small intragenic deletions/insertions and missense, nonsense, and splice site variants.

Gene-targeted deletion/duplication analysis may be performed; however, since POIKTMP likely occurs as the result of a dominant-negative genetic mechanism and since large intragenic deletions or duplications have not been reported, testing for intragenic deletions or duplications is unlikely to identify a disease-causing variant (see Molecular Genetics).

A multigene panel that includes FAM111B and other genes of interest (see Differential Diagnosis) may also be considered. Note: (1) The genes included in the panel and the diagnostic sensitivity of the testing used for each gene vary by laboratory and are likely to change over time. (2) Some multigene panels may include genes not associated with the condition discussed in this GeneReview (e.g., RECQL4, USB1, FERMT1); thus, clinicians need to determine which multigene panel provides the best opportunity to identify the genetic cause of the condition while limiting identification of pathogenic variants in genes that do not explain the underlying phenotype. (3) Methods used in a panel may include sequence analysis, deletion/duplication analysis, and/or other non-sequencing-based tests.

For an introduction to multigene panels click here. More detailed information for clinicians ordering genetic tests can be found here.

Option 2

Comprehensive genomic testing does not require the clinician to determine which gene is likely involved. Exome sequencing is most commonly used; genome sequencing is also possible.

For an introduction to comprehensive genomic testing click here. More detailed information for clinicians ordering genomic testing can be found here.

Table 1.

Molecular Genetic Testing Used in Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis

Gene 1MethodProportion of Probands with a Pathogenic Variant 2 Detectable by Method
FAM111B Sequence analysis 3100% 4
Gene-targeted deletion/duplication analysis 5None reported 6
1.
2.

See Molecular Genetics for information on variants detected in this gene.

3.

Sequence analysis detects variants that are benign, likely benign, of uncertain significance, likely pathogenic, or pathogenic. Variants may include small intragenic deletions/insertions and missense, nonsense, and splice site variants; typically, exon or whole-gene deletions/duplications are not detected. For issues to consider in interpretation of sequence analysis results, click here.

4.
5.

Gene-targeted deletion/duplication analysis detects intragenic deletions or duplications. Methods used may include quantitative PCR, long-range PCR, multiplex ligation-dependent probe amplification (MLPA), and a gene-targeted microarray designed to detect single-exon deletions or duplications.

6.

The spectrum of variants detected in affected individuals and functional studies [Author, unpublished observations] suggest a dominant-negative mechanism of disease; therefore, deletion/duplication testing is unlikely to detect a disease-causing variant.

Clinical Characteristics

Clinical Description

To date, 31 individuals have been identified with a pathogenic variant in FAM111B [Mercier et al 2013, Mercier et al 2015, Seo et al 2016, Takeichi et al 2017, Goussot et al 2017, Kazlouskaya et al 2018, Zhang et al 2019, Chen et al 2019, Chasseuil et al 2019, Dokic et al 2020]. The following description of the phenotypic features associated with this condition is based on these reports.

Individuals with hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) can exhibit few or many of the associated clinical features. The severity of the features (e.g., skin or muscle abnormalities) can vary. Intrafamilial clinical variability has been observed [Khumalo et al 2006, Seo et al 2016].

Skin

Skin abnormalities are the earliest findings. Of note, skin lesions – particularly facial poikiloderma – improve with time.

Poikiloderma appears during early infancy, typically in the first six months. It is mainly localized to the face (Figure 1). Transient exacerbations of facial erythema are seen following sun exposure. Mottled pigmentation is also a constituent part of poikiloderma.

Hypohidrosis with heat intolerance is observed in most.

Lymphedema of the lower and/or upper extremities may be present in childhood and is usually mild; it can be complicated by episodes of cellulitis.

Chronic erythematous and scaly skin lesions described as eczema-like, ichthyosis-like, or psoriasis-like lesions are often observed on the extremities.

Sclerosis of the digits and mild palmoplantar keratoderma may also be observed.

Hair/nails. Sparse scalp hair and sparse or absent eyelashes and/or eyebrows of variable severity are found in almost all affected individuals. Four affected individuals had mild nail dysplasia.

Muscle

Muscle contractures are usually seen in childhood and can be present as early as age two years. The most commonly affected muscles are the triceps surae, leading to a shortening of the Achilles tendons and varus deformities of the feet. Contractures of upper limbs (biceps brachii and carpal extensors) are also observed.

Myopathy. The majority of affected individuals develop progressive weakness of the proximal and distal muscles of all four limbs; the first manifestations (observed in lower limbs) are proximal rather than distal. Variability of muscle weakness ranges from loss of ambulation in childhood to absence of symptoms in adulthood [Mercier et al 2013, Mercier et al 2015, Seo et al 2016, Takeichi et al 2017].

Muscle weakness is generally associated with muscle atrophy and sometimes thoracolumbar scoliosis.

Serum creatine kinase is either normal or slightly increased. When performed, electromyography may show a normal or myopathic pattern.

Lung

Recurrent bronchitis can be observed. Abnormal lung function with restrictive pulmonary disease is common.

Some adults develop progressive interstitial pulmonary fibrosis, manifest as progressive breathlessness and dry cough; it can be life threatening within three to four years after the first respiratory symptoms appear.

Gastrointestinal

Pancreatic exocrine insufficiency (common in affected individuals) typically begins in childhood. Manifestations include fatty stools and diarrhea leading to chronic malabsorption of fats and lipid-soluble vitamins if not treated. Diagnosis is confirmed based on fecal elastase deficiency.

Liver impairment (reported in a few affected individuals) manifests initially as mildly elevated transaminases, alkaline phosphatase, gamma-glutamyl transferase, and/or bilirubin. One individual had hepatomegaly and cholestasis [Mercier et al 2013, Mercier et al 2015]. Another individual reported has transaminitis and lymphocytic ductulitis [Dokic et al 2020].

Other Features

Relative short stature and/or poor weight gain associated with delayed puberty have been reported.

Hematologic findings include eosinophilia or mild thrombocytopenia in some. Bone marrow hypocellularity was reported in a multiplex family [Seo et al 2016].

Hypothyroidism was described in a girl age 14 years [Takeichi et al 2017].

Eye. Cataract was reported in a girl age 13 years [Mercier et al 2015].

Cognitive development and function are normal. Of note, one individual had schizophrenia [Mercier et al 2015], which could be an incidental association.

Histopathology

Muscle histology shows extensive fatty infiltration. Residual muscle tissue is composed of fragmented muscle fascicles with either normal fibers or atrophic fibers with central nuclei (Figure 4 A-D). No neuropathic features (i.e., normal ATPase pattern) or mitochondrial network abnormalities are found on histochemistry or immunolabeling. Western blot analysis can show a secondary reduction of calpain.

Figure 4. A-D.

Figure 4

A-D. Muscle histology: A, B. Fatty tissue, fragmented muscle fascicles next to normal fascicles

Skin histology shows a characteristic pattern of epidermal atrophy with collagen sclerosis and elastic degeneration in the superficial and deep dermis. Elastic globes in the papillary dermis are associated with a diffuse mild collagen sclerosis (Figure 4 E-F).

Postmortem findings of one affected member of a South African family revealed diffuse fatty infiltration and fibrosis of organs including the lungs, esophagus, and pancreas [Khumalo et al 2006].

Genotype-Phenotype Correlations

POIKTMP is most frequently caused by heterozygosity for missense FAM111B pathogenic variants in the predicted trypsin-like cysteine/serine peptidase domain of the protein, in particular in the loop of the functional domain.

Further studies are needed to confirm these preliminary genotype-phenotype correlations.

Penetrance

To the authors' knowledge the penetrance of POIKTMP is 100%, with occurrence of skin features in early childhood.

Prevalence

The prevalence of POIKTMP is unknown. The condition is thought to be ubiquitous and is likely underdiagnosed.

Differential Diagnosis

Disorders with phenotypic similarity to hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) are summarized in Table 2. Notably, unlike POIKTMP, the disorders in Table 2 are not associated with muscle contractures, myopathy, or exocrine pancreatic insufficiency.

Table 2.

Genes and Disorders to Consider in the Differential Diagnosis of Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis

Gene(s)DisorderMOIOverlapping FeaturesAdditional Distinguishing Features
ANAPC1
RECQL4 		Rothmund Thomson syndrome (RTS)AREarly-onset poikiloderma, hypotrichosis, palmoplantar keratodermaRTS is assoc w/skeletal & dental abnormalities.
FERMT1 Kindler syndrome ARDiffuse poikiloderma w/striate & reticulate atrophy; widespread eczema-like dermatitis; keratotic papules of hands, feet, elbows, & knees; marked photosensitivityKindler syndrome is assoc w/skin fragility w/bullae on extremities at birth & after minor trauma, webbing of fingers & toes, & esophageal & urethral strictures.
USB1 Poikiloderma with neutropenia (PN)AREarly-onset poikiloderma & hematologic featuresPN is assoc w/distal-proximal limb & central body rash, hyperkeratotic nails, & recurrent infections. PN is not assoc w/photo- or heat sensitivity.

Hereditary sclerosing poikiloderma (HSP) of Weary (OMIM 173700), a disorder of unknown genetic cause, can also be considered in the differential diagnosis of POIKTMP. Like POIKTMP, HSP of Weary is associated with poikiloderma and sclerosis of palms and soles. Unlike POIKTMP, HSP of Weary is also known to be associated with linear sclerotic bands, subcutaneous calcifications, and valvular heart disease. HSP of Weary can be further distinguished from POIKTMP by the absence of muscle contractures, myopathy, and exocrine pancreatic insufficiency.

Management

Evaluations Following Initial Diagnosis

To establish the extent of disease and needs in an individual diagnosed with hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP), the evaluations summarized in Table 3 (if not performed as part of the evaluation that led to the diagnosis) are recommended.

Table 3.

Recommended Evaluations Following Initial Diagnosis in Individuals with Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis

System/ConcernEvaluationComment
Skin Dermatologic eval
Muscle PT assessmentMuscle MRI to evaluate for progressive muscle involvement is optional.
Lung Eval by pulmonary specialists incl pulmonary function testing to evaluate for restrictive lung disease &/or pulmonary fibrosis
Pancreas Fecal elastase level if steatorrhea is present
Liver Serum transaminases (SGOT, SGPT), alkaline phosphatase, & gamma-glutamyl transferase
Growth/
Nutrition 		Growth assessment for short stature &/or poor weight gain
Hematologic Complete blood count w/differential
Eye Ophthalmologic exam to evaluate for cataracts or other ocular abnormalities
Genetic
counseling 		By genetics professionals 1To inform patients & their families re nature, MOI, & implications of POIKTMP in order to facilitate medical & personal decision making
Family support
& resources 		Assess:

MOI = mode of inheritance; PT = physical therapy

1.

Medical geneticist, certified genetic counselor, certified advanced genetic nurse

Treatment of Manifestations

Table 4.

Treatment of Manifestations in Individuals with Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis

Manifestation/
Concern		TreatmentConsiderations/Other
Poikiloderma
  • Avoidance of excessive sun exposure
  • Use of sunscreens w/both UVA & UVB protection
Pulsed dye laserCan be discussed w/older patients for cosmetic management of telangiectatic component of the rash, but no data on its use are available.
Hypohidrosis
  • Avoidance of excessive heat exposure
  • Control of fever
Especially in 1st yrs of life to prevent overheating
Lymphedema
  • Manual lymphatic drainage
  • Compression
Eczema-like
lesions 		Topical treatment (e.g., emollients, topical steroids)
Muscle
contractures
& weakness
  • PT & exercise to promote mobility & prevent contractures
  • Calcium & vitamin D supplements may also be warranted in those w/muscle weakness to prevent osteopenia.
Lung disease
  • Use of self-inflating manual ventilation bag or mechanical insufflation-exsufflation device if needed
  • Noninvasive ventilation if needed
Pancreatic
exocrine
insufficiency 		Pancreatic enzyme supplementation
Liver
impairment 		Treatment of cholestasis w/ursodeoxycholic acid
Growth/
Nutrition 		Food supplement or enteral feeding as needed for poor weight gain
Cataract Surgical removal of visually significant cataracts

PT = physical therapy

Surveillance

Table 5.

Recommended Surveillance for Individuals with Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis

System/ConcernEvaluationFrequency
Dermatologic Dermatologic eval for poikiloderma, lymphedema of the limbs, eczema-like lesions, changes in nails & hairAnnually &/or as needed
Orthopedic
complications
  • PT assessment for muscle weakness or contractures
  • Orthopedic eval for contractures (w/attn to Achilles tendon contractures) & scoliosis
Pulmonary disease Pulmonary function testing (FVC +/- chest CT scan w/DLCO)
Liver dysfunction Serum transaminases (SGOT, SGPT), alkaline phosphatase, & gamma-glutamyl transferase
Endocrine
complications
  • Blood ionogram (Na+, K+, Cl-HCO3-, Ca2+)
  • TSH
Thrombocytopenia,
eosinophilia 		Complete blood count w/differential
Cataract Ophthalmologic exam

DLCO = diffusing capacity of the lungs for carbon monoxide; FVC = forced vital capacity; PT = physical therapy

Agents/Circumstances to Avoid

Avoid the following:

  • Excessive sun exposure, which may exacerbate the rash
  • Exposure to heat because of heat intolerance secondary to hypohidrosis

Evaluation of Relatives at Risk

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

Therapies Under Investigation

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

Genetic Counseling

Genetic counseling is the process of providing individuals and families with information on the nature, mode(s) of inheritance, and implications of genetic disorders to help them make informed medical and personal decisions. The following section deals with genetic risk assessment and the use of family history and genetic testing to clarify genetic status for family members; it is not meant to address all personal, cultural, or ethical issues that may arise or to substitute for consultation with a genetics professional. —ED.

Mode of Inheritance

Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) is inherited in an autosomal dominant manner.

Risk to Family Members

Parents of a proband

  • Approximately 50% of individuals diagnosed with POIKTMP have an affected parent.
  • Approximately 50% of individuals diagnosed with POIKTMP have the disorder as the result of a de novo FAM111B pathogenic variant.
  • If the proband appears to be the only affected family member (i.e., a simplex case), molecular genetic testing is recommended for the parents of the proband to confirm their genetic status and to allow reliable recurrence risk counseling.
  • If the pathogenic variant identified in the proband is not identified in either parent and parental identity testing has confirmed biological maternity and paternity, the following possibilities should be considered:

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

  • If a parent of the proband is affected and/or is known to have the pathogenic variant identified in the proband, the risk to the sibs of inheriting the pathogenic variant is 50%. Although all sibs who inherit a FAM111B pathogenic variant are expected to develop manifestations of the disorder, intrafamilial clinical variability has been observed (see Clinical Description).
  • If the FAM111B pathogenic variant detected in the proband cannot be detected in the leukocyte DNA of either parent, the recurrence risk to sibs is estimated to be 1% because of the theoretic possibility of parental germline mosaicism [Rahbari et al 2016].
  • If the parents have not been tested for the FAM111B pathogenic variant but are clinically unaffected, the risk to the sibs of a proband appears to be low. However, sibs of a proband with clinically unaffected parents are still presumed to be at increased risk for POIKTMP because of the theoretic possibility of parental germline mosaicism.

Offspring of a proband. Each child of an individual with POIKTMP has a 50% chance of inheriting the FAM111B pathogenic variant.

Other family members. The risk to other family members depends on the status of the proband's parents: if a parent has the FAM111B pathogenic variant, his or her family members may be at risk.

Related Genetic Counseling Issues

Family planning

  • The optimal time for determination of genetic risk and discussion of the availability of prenatal/preimplantation genetic testing is before pregnancy.
  • It is appropriate to offer genetic counseling (including discussion of potential risks to offspring and reproductive options) to young adults who are affected or at risk.

Prenatal Testing and Preimplantation Genetic Testing

Once the FAM111B pathogenic variant has been identified in an affected family member, prenatal and preimplantation genetic testing are possible.

Differences in perspective may exist among medical professionals and within families regarding the use of prenatal testing. While most centers would consider use of prenatal testing to be a personal decision, discussion of these issues may be helpful.

Resources

GeneReviews staff has selected the following disease-specific and/or umbrella support organizations and/or registries for the benefit of individuals with this disorder and their families. GeneReviews is not responsible for the information provided by other organizations. For information on selection criteria, click here.

Molecular Genetics

Information in the Molecular Genetics and OMIM tables may differ from that elsewhere in the GeneReview: tables may contain more recent information. —ED.

Table A.

Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis: Genes and Databases

GeneChromosome LocusProteinHGMDClinVar
FAM111B 11q12​.1 Serine protease FAM111B FAM111B FAM111B

Data are compiled from the following standard references: gene from HGNC; chromosome locus from OMIM; protein from UniProt. For a description of databases (Locus Specific, HGMD, ClinVar) to which links are provided, click here.

Table B.

OMIM Entries for Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis (View All in OMIM)

615584FAMILY WITH SEQUENCE SIMILARITY 111, MEMBER B; FAM111B
615704POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP

Molecular Pathogenesis

The FAM111B protein is predicted to contain a trypsin-like cysteine/serine peptidase domain. A role in DNA replication is suggested [Aviner et al 2015].

Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) is most frequently caused by heterozygosity for missense FAM111B pathogenic variants in the predicted trypsin-like cysteine/serine peptidase domain of the protein, in particular in the loop of the functional domain.

Mechanism of disease causation. The mechanism of disease for POIKTMP is not known; however, the spectrum of pathogenic variants and functional studies suggest a dominant-negative mechanism [Mercier et al 2015; Author, unpublished data].

Table 6.

Notable FAM111B Pathogenic Variants

Reference SequencesDNA Nucleotide ChangePredicted Protein ChangeComment [Reference]
NM_198947​.3
NP_945185​.1 		c.1261_1263delAAGp.Lys421delMay be assoc w/less severe extracutaneous phenotype [Khumalo et al 2006, Mercier et al 2013, Mercier et al 2015, Seo et al 2016, Takeichi et al 2017]. Further studies are needed.
c.1247T>Cp.Phe416Ser
c.1289A>Cp.Gln430Pro
c.1861T>Gp.Tyr621Asp
c.1874C>Ap.Thr625Asn
c.1879A>Gp.Arg627Gly
c.1881A>Tp.Arg627Ser
c.1883G>Ap.Ser628Asn
c.1884T>Ap.Ser628Asn

Variants listed in the table have been provided by the authors. GeneReviews staff have not independently verified the classification of variants.

GeneReviews follows the standard naming conventions of the Human Genome Variation Society (varnomen​.hgvs.org). See Quick Reference for an explanation of nomenclature.

Chapter Notes

Author Notes

Areas of interest/inquiry:

  • Prof Sandra Mercier, MD, PhD, clinician geneticist; Dr Sébastien Barbarot, MD, PhD, dermatologist: diagnosis and clinical follow up of patients with POIKTMP
  • Sébastien Küry, DVM, PhD: FAM111B molecular diagnosis

Prof Sandra Mercier and Dr Sébastien Küry are part of the Inserm UMR 1087 / CNRS UMR 6291 research team where functional studies are underway to understand the pathophysiology of the disease and find therapeutic approaches.

Contact: sandra.mercier@chu-nantes.fr

Acknowledgments

We thank the families and patients for their cooperation and support.

Revision History

  • 9 September 2021 (sm) Revision: nucleotide variant correction: c.1881A>T
  • 5 August 2021 (sw) Comprehensive update posted live
  • 13 October 2016 (bp) Review posted live
  • 1 February 2016 (sm) Original submission

References

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