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Spinocerebellar ataxia type 31
rareSpinocerebellar ataxia type 31 (SCA31) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the late-onset of cerebral ataxia, dysarthria and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense and hearing difficulties.
- Identifiers
- MONDO:0007296 OMIM:117210Orphanet:217012
- Causal genes
- BEAN1
- Also known as
- SCA31 · spinocerebellar ataxia 16q22-linked · spinocerebellar ataxia 31
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