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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • Fructose - »õâ A monosaccharide in sweet fruits and honey that is soluble in water, alcohol, or ether. It is used as a preservative and an intravenous infusion in parenteral feeding.
    Synonyms : Apir Levulosa, Baxter Brand of Fructose, Bieffe Brand of Fructose, Braun Brand of Fructose, Ern Brand of Fructose, Fleboplast Levulosa, Fresenius Kabi Brand of Fructose, Grifols Brand of Fructose, Instituto Farmacologico Brand of Fructose, Levulosa, Levulosa Ife
  • Fructose Intolerance - »õâ An autosomal recessive fructose metabolism disorder due to deficient fructose-1-phosphate aldolase (EC 2.1.2.13) activity, resulting in accumulation of fructose-1-phosphate. The accumulated fructose-1-phosphate inhibits glycogenolysis and gluconeogenesis, causing severe hypoglycemia following ingestion of fructose. Prolonged fructose ingestion in infants leads ultimately to hepatic failure and death. Patients develop a strong distaste for sweet food, and avoid a chronic course of the disease by remaining on a fructose- and sucrose-free diet.
    Synonyms : Fructose Intolerances, Intolerance, Fructose, Intolerances, Fructose
  • Fructose Metabolism, Inborn Errors - »õâ Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test.
    Synonyms :
  • Fructose-1,6-Diphosphatase Deficiency - »õâ An autosomal recessive fructose metabolism disorder due to absent or deficient fructose-1,6-diphosphatase activity. Gluconeogenesis is impaired, resulting in accumulation of gluconeogenic precursors (e.g., amino acids, lactate, ketones) and manifested as hypoglycemia, ketosis, and lactic acidosis. Episodes in the newborn infant are often lethal. Later episodes are often brought on by fasting and febrile infections. As patients age through early childhood, tolerance to fasting improves and development becomes normal.
    Synonyms : Deficiency, Hexosediphosphatase, Fructose 1, 6 Diphosphatase Deficiency, Fructosediphosphatase Deficiency, Deficiencies, Fructose-1, 6-Bisphosphatase, Deficiencies, Fructose-1, 6-Diphosphatase, Deficiencies, Fructose-Biphosphatase
  • Fructose-Bisphosphatase - »õâ An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.
    Synonyms : D-Fructose-1, 6-Bisphosphate 1-Phosphohydrolase, FDPase, Fructose-1, 6-Biphosphatase, 1-Phosphohydrolase, D-Fructose-1, 6-Bisphosphate, D Fructose 1, 6 Bisphosphate 1 Phosphohydrolase, Fructose 1, 6 Biphosphatase, Fructose 1, 6 Bisphosphatase
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 1
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