Catalog

Spinocerebellar ataxia type 26

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 26 – http://id.who.int/icd/entity/586976339

Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar ataxia type 3, described to date in patients from one American family of Norwegian descent, and characterised by late-onset and slowly progressive gait ataxia, and eye movement problems.