Infantile glycine encephalopathy

MONDO:0017354

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

26 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by