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Spinocerebellar ataxia type 32

rare

Spinocerebellar ataxia type 32 (SCA32) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by ataxia, cognitive impairment and azoospermia in males.

Identifiers
MONDO:0013486 OMIM:613909Orphanet:276183
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
cerebellar ataxia with azoospermia and intellectual disability · SCA32 · spinocerebellar ataxia 32

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