Spinocerebellar ataxia type 38

MONDO:0014417

Spinocerebellar ataxia type 38 (SCA38) is a subtype of autosomal dominant cerebellar ataxia type 3 characterized by the adult-onset (average age: 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplopia and axonal neuropathy.

Also known as: SCA38, spinocerebellar ataxia type 38, spinocerebellar ataxia 38

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 38 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Disorder of phospholipids, sphingolipids and fatty acids biosynthesis (15) ↑ Autosomal dominant cerebellar ataxia type III (9)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 38 (0)

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