Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Spinocerebellar ataxia type 26

MONDO:0012246

Spinocerebellar ataxia type 26 (SCA26) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities.

Also known as: SCA26, spinocerebellar ataxia type 26, spinocerebellar ataxia 26

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 26 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by