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Up to: Mitochondrial oxidative phosphorylation disorder · Pontocerebellar hypoplasia

Pontocerebellar hypoplasia type 6

Pontocerebellar hypoplasia type 6 (PCH6) is a rare form of pontocerebellar hypoplasia characterized clinically at birth by hypotonia, clonus, epilepsy impaired swallowing and from infancy by progressive microencephaly, spasticity and lactic acidosis.

2 trials tagged with this condition →

This condition has no sub-types.