Neonatal glycine encephalopathy

MONDO:0017353

Neonatal glycine encephalopathy is a frequent, usually severe form of glycine encephalopathy (GE) characterized by coma, apnea, hypotonia, seizure and myoclonic jerks in the neonatal period, and subsequent developmental delay.

Also known as: classic glycine encephalopathy, neonatal NKH, neonatal non-ketotic hyperglycinemia

0 clinical trials for this condition and its sub-types, 0 tagged with Neonatal glycine encephalopathy itself.

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↑ Glycine encephalopathy (0)

Including sub-types (0) Tagged with Neonatal glycine encephalopathy (0)

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