About The Medical Condition Type II Nonketotic Hyperglycinemia
Find the definition of the medical term Type II Nonketotic Hyperglycinemia. Type II Nonketotic Hyperglycinemia defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Type II Nonketotic Hyperglycinemia
| Type II Nonketotic Hyperglycinemia Medical Condition |
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What's The Definition Of The Medical Condition Type II Nonketotic Hyperglycinemia?
An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system; an enzyme system with four components: P-, T-, H-, and L-proteins. Deficiency of the P-protein is the most prevalent form. Neonatal and juvenile presentations have been reported. Neonatal onset is more common and may be fatal. Clinical features include SEIZURES; hypotonia; APNEA; and COMA. When the illness presents in childhood there tends to be an associated progressive DEMENTIA accompanied by extrapyramidal signs. (Menkes, Textbook of Child Neurology, 5th ed, p46; Jpn J Hum Genet 1997 Mar;42(1):13-22)
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