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Up to: Disorder of phospholipids, sphingolipids and fatty acids biosynthesis · Autosomal dominant cerebellar ataxia type III
Spinocerebellar ataxia type 38
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.
This condition has no sub-types.