Spinocerebellar ataxia type 5

MONDO:0010848

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.

Also known as: SCA5, spinocerebellar ataxia type 5, spinocerebellar ataxia 5

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 5 itself.

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