Spinocerebellar ataxia type 5

MONDO:0010848

Spinocerebellar ataxia type 5 (SCA5) is a rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.

Also known as: SCA5, spinocerebellar ataxia type 5, spinocerebellar ataxia 5

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 5 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 III (9)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 5 (0)

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