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Spinocerebellar ataxia type 4

rare

Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by ataxia with sensory neuropathy.

Identifiers
MONDO:0010847 OMIM:600223Orphanet:98765
Causal genes
ZFHX3
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA4 · spinocerebellar ataxia 4 · spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy

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