Spinocerebellar ataxia type 3
Machado-Joseph disease is an autosomal dominant neuromuscular degenerative disease.
The clinical features are primarily cerebellar ataxia and ophthalmoplegia.
Machado-Joseph disease is also termed spinocerebellar ataxia type 3.
Related pages
Create an account to add page annotations
Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page