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Spinocerebellar ataxia type 23

rare

Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.

Identifiers
MONDO:0012449 OMIM:610245Orphanet:101108
Causal genes
PDYN
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA23 · spinocerebellar ataxia 23

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