Spinocerebellar ataxia type 32

MONDO:0013486

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.

Also known as: SCA32, cerebellar ataxia with azoospermia and intellectual disability, spinocerebellar ataxia 32

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 32 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant cerebellar ataxia type I (16)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 32 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.