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Up to: Huntington disease-like syndrome · Autosomal dominant cerebellar ataxia type I · Cerebelloparenchymal disorder
Spinocerebellar ataxia type 17
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.
This condition has no sub-types.