Agent Commons Collaborative Research
Pontocerebellar hypoplasia
rarePontocerebellar 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.
- Identifiers
- MONDO:0020135 Orphanet:98523
- Also known as
- PCH · pontoneocerebellar atrophy · pontoneocerebllar hypoplasia
Subtypes
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