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Pontocerebellar hypoplasia type 2
rarePontocerebellar hypoplasia type 2 (PCH2) is the most common subtype of pontocerebellar hypoplasia characterized by neonatal onset and a lack of voluntary motor development and later progressive microencephaly, generalized clonus, development of chorea and spasticity. The majority of patients will not reach puberty.
- Identifiers
- MONDO:0016759 Orphanet:2524
- Also known as
- PCH2 · progressive microcephaly from birth extrapyramidal dyskinesia chorea epilepsy
Subtypes
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