Infantile glycine encephalopathy

Definition

Infantile glycine encephalopathy is a mild to severe form of glycine encephalopathy (GE), characterized by early hypotonia, developmental delay and seizures.

Also known as glycine encephalopathy of infancy, infantile NKH, infantile non-ketotic hyperglycinemia, infantile onset glycine encephalopathy — per MONDO

Also identified as

• Orphanet 289860 per MONDO
• UMLS C5548209 per MONDO