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Infantile glycine encephalopathy
rareInfantile glycine encephalopathy is a mild to severe form of glycine encephalopathy (GE), characterized by early hypotonia, developmental delay and seizures.
- Identifiers
- MONDO:0017354 Orphanet:289860
- Part of
- Glycine encephalopathy
- Also known as
- glycine encephalopathy of infancy · infantile NKH · infantile non-ketotic hyperglycinemia · infantile onset glycine encephalopathy
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