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Pontocerebellar hypoplasia type 2

rare

Pontocerebellar 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.

Also known as
PCH2 · progressive microcephaly from birth extrapyramidal dyskinesia chorea epilepsy
Disease Subtypes
Pontocerebellar hypoplasia type 2A
Pontocerebellar hypoplasia type 2B
Pontocerebellar hypoplasia type 2C
Pontocerebellar hypoplasia type 2D
Pontocerebellar hypoplasia, type 2F

Rare disease

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