Catalog
Glycine encephalopathy
Link to WHO Definition
Glycine encephalopathy – http://id.who.int/icd/entity/1491869639
Isolated nonketotic hyperglycinemia is an inborn disorder of glycine metabolism whose onset is generally neonatal with coma, severe hypotonia, myoclonic seizures, and microcephaly, usually progressing to severe intellectual deficit and tetrapyramidal syndrome.