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Spinocerebellar ataxia type 26
rareSpinocerebellar 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.
- Identifiers
- MONDO:0012246 OMIM:609306Orphanet:101112
- Causal genes
- EEF2
- Also known as
- SCA26 · spinocerebellar ataxia 26
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