(Q56013977)
English
neonatal glycine encephalopathy
Neonatal glycine encephalopathy is a frequent, usually severe form of glycine encephalopathy (GE; see this term) characterized by coma, apnea, hypotonia, seizure and myoclonic jerks in the neonatal period, and subsequent developmental delay
- Neonatal non-ketotic hyperglycinemia
- Classic glycine encephalopathy
- Neonatal NKH
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