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intestinal malabsorption

См. также в других словарях:

  • Malabsorption — Classification and external resources Whipple s disease: Alcian blue with apparently eosin counterstain enlarged villus with many macrophages ICD 10 …   Wikipedia

  • malabsorption — [ malapsɔrpsjɔ̃ ] n. f. • av. 1969; de 2. mal et absorption ♦ Méd. Trouble du processus d absorption des aliments à travers la muqueuse intestinale. ● malabsorption nom féminin Trouble du processus d absorption des aliments à travers la muqueuse… …   Encyclopédie Universelle

  • Intestinal pseudoobstruction — Classification and external resources ICD 9 560.89 OMIM 155310 DiseasesDB …   Wikipedia

  • malabsorption syndrome — n a syndrome resulting from malabsorption that is typically characterized by weakness, diarrhea, muscle cramps, edema, and loss of weight * * * any of a group of disorders characterized by subnormal absorption of dietary constituents, and thus… …   Medical dictionary

  • malabsorption — Imperfect, inadequate, or otherwise disordered gastrointestinal absorption. congenital selective glucose and galactose m. an inherited disorder in which d glucose and d galactose accumulate in the intestinal lumen and exert an osmotic …   Medical dictionary

  • Intestinal — Intestin Dessin simplifié du système digestif (manuscrit persan du XVIIe écrit par Mansur ibn Muhammad Ahmad, bibliothèque de Majles, Téhéran) …   Wikipédia en Français

  • Glucose-galactose malabsorption — Classification and external resources ICD 10 E74.3 ICD 9 271.3 …   Wikipedia

  • Fructose malabsorption — Classification and external resources Fructose ICD 10 E …   Wikipedia

  • Hereditäre Folat-Malabsorption — Klassifikation nach ICD 10 D52.8 Sonstige Folsäure Mangelanämien …   Deutsch Wikipedia

  • ANGOR INTESTINAL — De même que l’angine de poitrine est la traduction d’une ischémie aiguë myocardique, l’angor intestinal est la traduction clinique d’une ischémie aiguë intestinale. C’est une douleur abdominale intense survenant peu de temps après un repas et qui …   Encyclopédie Universelle

  • glucose-galactose malabsorption — an autosomal recessive disorder caused by mutation in the SLC5A1 (SGLT1) gene (locus: 22q13.1), which encodes the intestinal sodium/glucose cotransporter, resulting in defective intestinal glucose and galactose transport. It is characterized by… …   Medical dictionary

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