Catalog

Spinocerebellar ataxia type 4

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 4 – http://id.who.int/icd/entity/1686006145

Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy.

Parents

Autosomal dominant cerebellar ataxia type 1