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  2. Vanishing bile duct syndrome - Wikipedia

    en.wikipedia.org/wiki/Vanishing_Bile_Duct_Syndrome

    Vanishing bile duct syndrome is a loose collection of diseases leading to ... Alpha 1 antitrypsin deficiency; ... Treatment is supportive as it is not possible to ...

  3. Cholestasis - Wikipedia

    en.wikipedia.org/wiki/Cholestasis

    These signs and symptoms resolve on their own shortly after delivery, though they may reappear in subsequent pregnancies for 45–70% of women. [62] In the treatment of ICP, current evidence suggests ursodeoxycholic acid (UDCA), a minor secondary bile acid in humans, is the most effective drug for reducing pruritus and improving liver function ...

  4. Bile acid malabsorption - Wikipedia

    en.wikipedia.org/wiki/Bile_acid_malabsorption

    It has also been called bile acid-induced diarrhea, cholerheic or choleretic enteropathy, bile salt diarrhea or bile salt malabsorption. It can result from malabsorption secondary to gastrointestinal disease, or be a primary disorder, associated with excessive bile acid production. Treatment with bile acid sequestrants is often effective ...

  5. Malabsorption - Wikipedia

    en.wikipedia.org/wiki/Malabsorption

    Normally the human gastrointestinal tract digests and absorbs dietary nutrients with remarkable efficiency. A typical Western diet ingested by an adult in one day includes approximately 100 g of fat, 400 g of carbohydrate, 100 g of protein, 2 L of fluid, and the required sodium , potassium , chloride , calcium , vitamins , and other elements.

  6. Biliary atresia - Wikipedia

    en.wikipedia.org/wiki/Biliary_atresia

    The babies have homozygous deficiency of glutathione S transferase (GST) M1. [22] The aflatoxin damaged liver cells and bile duct cells are removed by neutrophil elastase [23] and by involvement of immune system mediators such as CCL-2 or MCP-1, tumor necrosis factor (TNF), interleukin-6 (IL-6), TGF-beta, endothelin (ET), and nitric oxide (NO ...

  7. Progressive familial intrahepatic cholestasis - Wikipedia

    en.wikipedia.org/wiki/Progressive_familial_intra...

    The defective phosphatidylcholine translocation leads to a lack of phosphatidylcholine in bile. Phosphatidylcholine normally chaperones bile acids, preventing damage to the biliary epithelium. The free or "unchaperoned" bile acids in bile of patients with MDR3 deficiency cause a cholangitis. Biochemically, this is of note, as PFIC-3 is ...

  8. Gallbladder disease - Wikipedia

    en.wikipedia.org/wiki/Gallbladder_disease

    Gallbladder diseases are diseases involving the gallbladder and is closely linked to biliary disease, with the most common cause being gallstones (cholelithiasis). [1] [2]The gallbladder is designed to aid in the digestion of fats by concentrating and storing the bile made in the liver and transferring it through the biliary tract to the digestive system through bile ducts that connect the ...

  9. Biliary dyskinesia - Wikipedia

    en.wikipedia.org/wiki/Biliary_dyskinesia

    When bile enters the duodenum (the first part of the small intestine), it aids in digesting the fat within food leaving the stomach. When the bile can not be properly propelled from the not-mechanically-obstructed gallbladder or can not flow out of the end of the common bile duct properly, there is a state of biliary dyskinesia.