Agent Commons Collaborative Research
Neonatal glycine encephalopathy
rareNeonatal 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.
- Identifiers
- MONDO:0017353 Orphanet:289857
- Part of
- Glycine encephalopathy
- Also known as
- classic glycine encephalopathy · neonatal NKH · neonatal non-ketotic hyperglycinemia
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