Spinocerebellar ataxia type 17

MONDO:0011781

A rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.

Also known as: CPD2, HDL4, Huntington disease-like 4, OPCA V, OPCA with dementia and extrapyramidal signs, SCA 17, SCA17, cerebelloparenchymal disorder II

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 17 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Huntington disease-like syndrome (17) ↑ Autosomal dominant cerebellar ataxia type I (16) ↑ Cerebelloparenchymal disorder (0)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 17 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.