- 尿内甘氨酸过多,高甘氨酸尿
- renal hyperglycinuria: 肾性高甘氨酸尿
- hyperglycistia: 组织糖分过多
- hyperglycinemias,nonketotic: 《英文msh词典》Hyperglycinemias,Nonketotic ; [入口词] Hyperglycinemias,Nonketotic ; [主题词] Hyperglycinemia,Nonketotic ; [英文释义] 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)
- hyperglycogenolysis: [医] 糖原分解过度
- hyperglycinemia,nonketotic,type iii: 《英文msh词典》Hyperglycinemia,Nonketotic,Type III ; [入口词] Hyperglycinemia,Nonketotic,Type III ; [主题词] Hyperglycinemia,Nonketotic ; [英文释义] 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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