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Infantile glycine encephalopathy
MONDO:0017354Infantile 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
0 clinical trials for this condition and its sub-types, 0 tagged with Infantile glycine encephalopathy itself.
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