Juvenile paralysis agitans of Hunt

MedGen UID:: 66768
•Concept ID:: C0238344
•: Disease or Syndrome

Synonym:	Parkinson disease, juvenile, of Hunt
SNOMED CT:	Juvenile paralysis agitans of Hunt (43647007); Paleostriatal syndrome (43647007); Neostriatal syndrome (43647007); Pallidal syndrome (43647007); Pallidal atrophy (43647007)

Monarch Initiative:	MONDO:0008193
OMIM®:	168100

Authors:
Lola Cook Shukla | Jeanine Schulze | Janice Farlow, et. al. view full author information

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVParkinson disease

Non-Neoplastic Disorder
- Non-Neoplastic Disorder by Special Category
  - Degenerative disorder
    - Degenerative disease of the central nervous system
      - Extrapyramidal disease
        Parkinson disease
        Juvenile paralysis agitans of Hunt

Recent clinical studies

Diagnosis

Basal Ganglia Atrophy as a Marker for Prodromal X-Linked Dystonia-Parkinsonism.

Hanssen H, Diesta CCE, Heldmann M, Dy J, Tantianpact J, Steinhardt J, Sauza R, Manalo HTS, Sprenger A, Reyes CJ, Tuazon R, Laabs BH, Domingo A, Rosales RL, Klein C, Münte TF, Westenberger A, Oropilla JQ, Brüggemann N
Ann Neurol 2023 May;93(5):999-1011. Epub 2023 Feb 17 doi: 10.1002/ana.26606. PMID: 36646669

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Therapy

Basal Ganglia Atrophy as a Marker for Prodromal X-Linked Dystonia-Parkinsonism.

See all (1)

MedGen

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Juvenile paralysis agitans of Hunt

Term Hierarchy

Recent clinical studies

Diagnosis

Therapy

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Reviews

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