Spinocerebellar ataxia type 11 (SCA11): An update.

Abstract excerpt

Spinocerebellar ataxias, also called autosomal dominant cerebellar ataxias, are a group of neurological genetic diseases characterised by chronic, progressive cerebellar ataxia. The clinical hallmark of spinocerebellar ataxia is the loss of balance and coordination, accompanied by slurred speech. Spinocerebellar ataxia type 11 is a rare subtype of spinocerebellar ataxia caused by mutations in the tau tubulin...

Topics

• Humans
• Cerebellar Ataxia
• Spinocerebellar Ataxias
• Spinocerebellar Degenerations
• Mutation
• Nervous System Diseases