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・ Glycobius
・ Glycocalyx
・ Glycochenodeoxycholate sulfotransferase
・ Glycochenodeoxycholic acid
・ Glycocholic acid
・ Glycoconjugate
・ Glycocyamine
・ Glycodeoxycholic acid
・ Glycogen
・ Glycogen body
・ Glycogen branching enzyme
・ Glycogen debranching enzyme
・ Glycogen phosphorylase
・ Glycogen phosphorylase isoenzyme BB
・ Glycogen storage disease
Glycogen storage disease type 0
・ Glycogen storage disease type I
・ Glycogen storage disease type II
・ Glycogen storage disease type III
・ Glycogen storage disease type IV
・ Glycogen storage disease type IX
・ Glycogen storage disease type V
・ Glycogen storage disease type VI
・ Glycogen storage disease type XI
・ Glycogen synthase
・ Glycogen synthase kinase
・ Glycogen-branching enzyme deficiency
・ Glycogenase
・ Glycogenesis
・ Glycogenic acanthosis


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Glycogen storage disease type 0 : ウィキペディア英語版
Glycogen storage disease type 0

Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme. Although glycogen synthase deficiency does not result in storage of extra glycogen in the liver, it is often classified with the Glycogen storage diseases because it is another defect of glycogen storage and can cause similar problems. Mutations in the liver isoform, GYS2, causes fasting hypoglycemia, high blood ketones, increased free fatty acids and low levels of alanine and lactate. Conversely, feeding in these patients results in hyperglycemia and hyperlactatemia.
There are two versions: the muscle version involves GYS1 and the liver version involves GYS2.
==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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