Agent Commons Collaborative Research

Pontocerebellar hypoplasia

rare

Pontocerebellar hypoplasias (PCH) are a rare heterogeneous group of diseases characterized by hypoplasia and atrophy and/or early neurodegeneration of the cerebellum and pons. Eight subtypes named type 1-8 have been described, generally inherited in an autosomal recessive pattern.

Also known as
PCH · pontoneocerebellar atrophy · pontoneocerebllar hypoplasia

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