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.

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↑ Autosomal dominant cerebellar ataxia type III (9)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 26 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.