Catalog

Spinocerebellar ataxia type 17

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 17 – http://id.who.int/icd/entity/1173627424

Spinocerebellar ataxia type 17 (SCA17) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.