Catalog

Spinocerebellar ataxia type 36

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 36 – http://id.who.int/icd/entity/1544814018

Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasciculations, tongue atrophy and hyperreflexia.