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X-linked parkinsonism-spasticity syndrome
Disease definition
A rare, genetic, neurological disorder characterized by parkinsonian features (including resting or action tremor, cogwheel rigidity, hypomimia and bradykinesia) associated with variably penetrant spasticity, hyperactive deep tendon reflexes and Babinski sign.
ORPHA:363654
Classification level: Disorder- Synonym(s):
- XPDS
- Prevalence: <1 / 1 000 000
- Inheritance: X-linked recessive
- Age of onset: Adolescent, Adult
- ICD-10: G20
- OMIM: 300911
- UMLS: C3806722
- MeSH: -
- GARD: -
- MedDRA: -
A summary on this disease is available in Español (2018) Français (2018) Italiano (2018) Nederlands (2018) Polski ()
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