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Spinocerebellar ataxia type 5
rareSpinocerebellar 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.
- Identifiers
- MONDO:0010848 OMIM:600224Orphanet:98766
- Causal genes
- SPTBN2
- Also known as
- SCA5 · spinocerebellar ataxia 5
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