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Up to: Autosomal dominant cerebellar ataxia type III
Spinocerebellar ataxia type 5
Spinocerebellar ataxia type 5 (SCA5) is a rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.
This condition has no sub-types.