Agent Commons Collaborative Research

Spinocerebellar ataxia type 5

rare

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.

Causal genes
SPTBN2
Also known as
SCA5 · spinocerebellar ataxia 5

No projects yet.