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  2. Disaccharidase - Wikipedia

    en.wikipedia.org/wiki/Disaccharidase

    Disaccharidases are glycoside hydrolases, enzymes that break down certain types of sugars called disaccharides into simpler sugars called monosaccharides.In the human body, disaccharidases are made mostly in an area of the small intestine's wall called the brush border, making them members of the group of "brush border enzymes".

  3. Malabsorption - Wikipedia

    en.wikipedia.org/wiki/Malabsorption

    Excessive flatus and abdominal bloating may reflect excessive gas production due to fermentation of unabsorbed carbohydrate, especially among patients with a primary or secondary disaccharidase deficiency, such as lactose intolerance or sucrose intolerance. Malabsorption of dietary nutrients and excessive fluid secretion by inflamed small ...

  4. Sucrose intolerance - Wikipedia

    en.wikipedia.org/wiki/Sucrose_intolerance

    Sucrose intolerance can also be caused by irritable bowel syndrome, aging, or small intestine disease (secondary sucrose intolerance). There are specific tests used to help determine if a person has sucrose intolerance. The most accurate test is the enzyme activity determination, which is done by biopsying the small intestine.

  5. Inborn errors of carbohydrate metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of...

    Hereditary fructose intolerance (HFI) results in poor feeding, failure to thrive, chronic liver disease and chronic kidney disease, and death. HFI is caused by a deficiency of fructose 1,6-biphosphate aldolase in the liver, kidney cortex and small intestine.

  6. Sucrase-isomaltase - Wikipedia

    en.wikipedia.org/wiki/Sucrase-isomaltase

    A deficiency is responsible for sucrose intolerance.Congenital sucrase-isomaltase deficiency (CSID), also called genetic sucrase-isomaltase deficiency (GSID), and sucrose intolerance, is a genetic, intestinal disorder that is caused by a reduction or absence of sucrase and isomaltase [13] Explanations for GSID include:

  7. List of ICD-9 codes 240–279: endocrine, nutritional and ...

    en.wikipedia.org/wiki/List_of_ICD-9_codes_240...

    Von Gierke's disease; McArdle's disease; Pompe's disease; 271.1 Galactosemia; 271.2 Hereditary fructose intolerance; 271.3 Intestinal disaccharidase deficiencies and disaccharide malabsorption. Lactose intolerance; Glucose intolerance; 271.4 Renal glycosuria; 271.8 Other specified disorders of carbohydrate transport and metabolism

  8. Sucrase - Wikipedia

    en.wikipedia.org/wiki/Sucrase

    With sucrose intolerance, the result of consuming sucrose is excess gas production and often diarrhea and malabsorption. Lactose intolerance is a similar condition that reflects an individual's inability to hydrolyze the disaccharide lactose. Sucrase is secreted by the tips of the villi of the epithelium in the small intestine.

  9. Disaccharide - Wikipedia

    en.wikipedia.org/wiki/Disaccharide

    Breaking apart a double sugar into its two monosaccharides is accomplished by hydrolysis with the help of a type of enzyme called a disaccharidase. As building the larger sugar ejects a water molecule, breaking it down consumes a water molecule. These reactions are vital in metabolism.