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Spinocerebellar ataxia type 36

rare

Spinocerebellar ataxia type 36 (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia.

Identifiers
MONDO:0013594 OMIM:614153Orphanet:276198
Causal genes
NOP56
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
Asidan · SCA36 · spinocerebellar ataxia 36

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