Neonatal glycine encephalopathy

Neonatal glycine encephalopathy

Definition

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 — per MONDO

Also identified as