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Up to: Hereditary skin disorder · Autosomal dominant cerebellar ataxia type I · Erythrokeratoderma
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.
This condition has no sub-types.