Catalog

Spinocerebellar ataxia type 6

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 6 – http://id.who.int/icd/entity/1056119281

Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene.