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  2. Primary biliary cholangitis - Wikipedia

    en.wikipedia.org/wiki/Primary_biliary_cholangitis

    Primary biliary cholangitis (PBC), previously known as primary biliary cirrhosis, is an autoimmune disease of the liver. [ 1 ] [ 2 ] [ 3 ] It results from a slow, progressive destruction of the small bile ducts of the liver, causing bile and other toxins to build up in the liver, a condition called cholestasis .

  3. Cholestatic pruritus - Wikipedia

    en.wikipedia.org/wiki/Cholestatic_pruritus

    Cholestatic pruritus is the sensation of itch due to nearly any liver disease, but the most commonly associated entities are primary biliary cholangitis, primary sclerosing cholangitis, obstructive choledocholithiasis, carcinoma of the bile duct, cholestasis (also see drug-induced pruritus), and chronic hepatitis C viral infection and other forms of viral hepatitis.

  4. Elevated alkaline phosphatase - Wikipedia

    en.wikipedia.org/wiki/Elevated_alkaline_phosphatase

    Skeletal involvement of other primary diseases: Osteomalacia, rickets, vitamin D deficiency (moderate rise) Malignant tumors (ALP originating from tumor) Renal disease (secondary hyperparathyroidism) Hyperthyroidism. [7] Other unlisted musculoskeletal conditions may also cause elevated alkaline phosphatase.

  5. Anti-mitochondrial antibody - Wikipedia

    en.wikipedia.org/wiki/Anti-mitochondrial_antibody

    Anti-mitochondrial antibodies (AMA) are autoantibodies, consisting of immunoglobulins formed against mitochondria, [1] primarily the mitochondria in cells of the liver.. The presence of AMA in the blood or serum of a person may be indicative of the presence of, or the potential to develop, the autoimmune disease primary biliary cholangitis (PBC; previously known as primary biliary cirrhosis).

  6. Bile acid - Wikipedia

    en.wikipedia.org/wiki/Bile_acid

    Structural or functional abnormalities of the biliary system result in an increase in bilirubin and in bile acids in the blood. Bile acids are related to the itching which is common in cholestatic conditions such as primary biliary cirrhosis (PBC), primary sclerosing cholangitis or intrahepatic cholestasis of pregnancy. [24]

  7. Cholestasis - Wikipedia

    en.wikipedia.org/wiki/Cholestasis

    For patients with primary biliary cholangitis, current guidelines recommend about 13–15 mg/kg of ursodeoxycholic acid as a first line treatment. [121] This drug stimulates biliary bicarbonate secretion, improves survival without having to resort to a liver transplantation, and is very well tolerated—making it an ideal treatment. [ 122 ]

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