Autosomal dominant cerebellar ataxia
This is a heterogeneous group of adult-onset progressive ataxias which have an autosomal dominant mode of inheritance. There is often a widespread neuronal degeneration which resembles multiple system atrophy.
There are three main clinical groups:
- spinocerebellar ataxia type 1
- spinocerebellar ataxia type 2
- Machado-Joseph syndrome
- cerebellar cortical degeneration
Related pages
Create an account to add page annotations
Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.