Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Autosomal dominant cerebellar ataxia type III
Spinocerebellar ataxia type 26
Spinocerebellar ataxia type 26 (SCA26) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities.
This condition has no sub-types.