Catalog

Spinocerebellar ataxia type 35

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 35 – http://id.who.int/icd/entity/1674449075

Spinocerebellar ataxia type 35 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, tremor, hyperreflexia and torticollis.