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.
Comprehensive, easy-to-understand information about this condition
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pontocerebellar hypoplasia type 4
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pontocerebellar hypoplasia type 5
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pontocerebellar hypoplasia type 6
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pontocerebellar hypoplasia type 2B
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