Pontocerebellar hypoplasia type 1A

Any non-syndromic pontocerebellar hypoplasia in which the cause of the disease is a mutation in the VRK1 gene.

Also known as: VRK1 non-syndromic pontocerebellar hypoplasia, non-syndromic pontocerebellar hypoplasia caused by mutation in VRK1, PCH1A, Pch1, pontocerebellar hypoplasia with anterior horn cell disease, pontocerebellar hypoplasia with infantile spinal muscular atrophy, pontocerebellar hypoplasia, type 1A

11 clinical trials for this condition and its sub-types, 0 tagged with Pontocerebellar hypoplasia type 1A itself.