Spinocerebellar ataxia type 34

A subtype of autosomal dominant cerebellar ataxia type I (ADCA type I), characterized by papulosquamous, ichthyosiform plaques on the limbs appearing shortly after birth and later manifestations including progressive ataxia, dysarthria, nystagmus and decreased reflexes.

Also known as: Erythrokeratodermia with Ataxia, SCA34, erythrokeratodermia with ataxia, spinocerebellar ataxia and erythrokeratodermia, spinocerebellar ataxia type 34, Giroux Barbeau syndrome, erythrokeratodermia - ataxia, spinocerebellar ataxia 34

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 34 itself.