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・ Glyceria grandis
・ Glyceria leptostachya
・ Glyceria maxima
・ Glyceria notata
・ Glutaminyl-tRNA synthase (glutamine-hydrolysing)
・ Glutamyl aminopeptidase
・ Glutamyl endopeptidase
・ Glutamyl endopeptidase II
・ Glutamyl-tRNA reductase
・ Glutaraldehyde
・ Glutarate-semialdehyde dehydrogenase
・ Glutarate—CoA ligase
・ Glutaredoxin
・ Glutaredoxin 2 (bacterial)
・ Glutaric acid
Glutaric acidemia type 2
・ Glutaric aciduria type 1
・ Glutarimide
・ Glutaronitrile
・ Glutaryl-7-aminocephalosporanic-acid acylase
・ Glutaryl-CoA
・ Glutaryl-CoA dehydrogenase
・ Glutaryl-CoA dehydrogenase (non-decarboxylating)
・ Glutathione
・ Glutathione amide reductase
・ Glutathione amide-dependent peroxidase
・ Glutathione dehydrogenase (ascorbate)
・ Glutathione disulfide
・ Glutathione gamma-glutamylcysteinyltransferase
・ Glutathione hydrolase


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Glutaric acidemia type 2 : ウィキペディア英語版
Glutaric acidemia type 2

Glutaric acidemia type 2 is an autosomal recessive metabolic disorder that is characterised by defects in the ability of the body to use proteins and fats for energy. Incompletely processed proteins and fats can build up, leading to a dangerous chemical imbalance called acidosis.
==Diagnosis==

Glutaric acidemia type 2 often appears in infancy as a sudden metabolic crisis, in which acidosis and low blood sugar (hypoglycemia) cause weakness, behavior changes, and vomiting. There may also be enlargement of the liver, heart failure, and a characteristic odor resembling that of sweaty feet. Some infants with glutaric acidemia type 2 have birth defects, including multiple fluid-filled growths in the kidneys (polycystic kidneys). Glutaric acidemia type 2 is a very rare disorder. Its precise incidence is unknown. It has been reported in several different ethnic groups.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Glutaric acidemia type 2」の詳細全文を読む



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