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Spinocerebellar ataxia type 25

rare

Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by cerebellar ataxia and prominent sensory neuropathy.

Identifiers
MONDO:0012103 OMIM:608703Orphanet:101111
Causal genes
PNPT1
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA25 · spinocerebellar ataxia 25

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