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Spinocerebellar ataxia type 35

rare

Spinocerebellar ataxia type 35 (SCA35) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, intention tremor, hyperreflexia and spasmodic torticollis.

Identifiers
MONDO:0013485 OMIM:613908Orphanet:276193
Causal genes
TGM6
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA35 · spinocerebellar ataxia 35

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