Spinocerebellar ataxia type 36

MONDO:0013594

Spinocerebellar ataxia type 36 (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia.

Also known as: Asidan, SCA36, spinocerebellar ataxia type 36, spinocerebellar ataxia 36

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 36 itself.

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Where it sits in the disease tree

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↑ Autosomal dominant cerebellar ataxia type I (16)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 36 (0)

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