Glycine encephalopathy

MONDO:0011612

Glycine encephalopathy (GE) is an inborn error of glycine metabolism characterized by accumulation of glycine in body fluids and tissues, including the brain, resulting in neurometabolic symptoms of variable severity.

Also known as: NKA, Nonketotic Hyperglycinemia, glycine encephalopathy, non-ketotic hyperglycinemia, nonketotic hyperglycinemia, GCE, GLYCINE encephalopathy, Glycine synthase deficiency

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

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by