Congenital disorders of intestinal digestion and absorption (sugars, proteins, lipids, ions) - Inserm - Institut national de la santé et de la recherche médicale Access content directly
Journal Articles Best Practice and Research: Clinical Gastroenterology Year : 2022

Congenital disorders of intestinal digestion and absorption (sugars, proteins, lipids, ions)

Abstract

Congenital diarrhea may result from 2 main different mechanisms: 1) osmotic diarrhea is caused by the non-digestion-absorption of nutrients leading to the non-absorbed nutrients going into the lumen, increasing the osmotic force and driving fluids; 2) secretory diarrhea induced by the inhibition of intestinal absorption of electrolytes, increasing electrolyte and water flux towards the intestinal lumen. The malabsorption of macronutrients (carbohydrates, proteins and lipids) induces energy deficiency with symptoms depending on the macronutrient: carbohydrates with watery acidic diarrhea; protein with rapid malnutrition, edema, and hypoalbuminemia; and lipids with malnutrition, steatorrhea and hypocholesterolemia. Ionic malabsorption (Cl and Na) is responsible for severe and rapid dehydration sometimes with prenatal abnormalities (polyhydramnios and bowel dilatation).
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Dates and versions

inserm-03754194 , version 1 (19-08-2022)

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N. Peretti, E. Mas. Congenital disorders of intestinal digestion and absorption (sugars, proteins, lipids, ions). Best Practice and Research: Clinical Gastroenterology, 2022, 56-57, pp.101785. ⟨10.1016/j.bpg.2022.101785⟩. ⟨inserm-03754194⟩
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