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Spinocerebellar ataxia type 31

rare

Spinocerebellar 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.

Causal genes
BEAN1
Also known as
SCA31 · spinocerebellar ataxia 16q22-linked · spinocerebellar ataxia 31

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