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  2. Exocrine pancreatic insufficiency - Wikipedia

    en.wikipedia.org/wiki/Exocrine_pancreatic...

    Exocrine pancreatic insufficiency (EPI) is the inability to properly digest food due to a lack or reduction of digestive enzymes made by the pancreas.EPI can occur in humans and is prevalent in many conditions [1] such as cystic fibrosis, [2] Shwachman–Diamond syndrome, [3] different types of pancreatitis, [4] multiple types of diabetes mellitus (Type 1 and Type 2 diabetes), [5] advanced ...

  3. Category:Pancreas disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Pancreas_disorders

    Generally, diseases outlined within the ICD-10 codes K85-K86 within Chapter XI: Diseases of the digestive system should be included in this category. Wikimedia Commons has media related to Diseases and disorders of pancreas .

  4. Pancreatic disease - Wikipedia

    en.wikipedia.org/wiki/Pancreatic_disease

    Exocrine pancreatic insufficiency (EPI) is the inability to properly digest food due to a lack of digestive enzymes made by the pancreas. EPI is found in humans affected by cystic fibrosis and Shwachman–Diamond syndrome. It is caused by a progressive loss of the pancreatic cells that make digestive enzymes.

  5. Lipoprotein lipase deficiency - Wikipedia

    en.wikipedia.org/wiki/Lipoprotein_lipase_deficiency

    Lipoprotein lipase deficiency is a genetic disorder in which a person has a defective gene for lipoprotein lipase, which leads to very high triglycerides, which in turn causes stomach pain and deposits of fat under the skin, and which can lead to problems with the pancreas and liver, which in turn can lead to diabetes.

  6. Johanson–Blizzard syndrome - Wikipedia

    en.wikipedia.org/wiki/Johanson–Blizzard_syndrome

    Pancreatic insufficiency and malabsorption can be managed with pancreatic enzyme replacement therapy, such as pancrelipase supplementation and other related methods. [1] Craniofacial and skeletal deformities may require surgical correction, using techniques including bone grafts and osteotomy procedures. [20]

  7. Hereditary pancreatitis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_pancreatitis

    Hereditary pancreatitis (HP) is an inflammation of the pancreas due to genetic causes. It was first described in 1952 by Comfort and Steinberg [1] but it was not until 1996 that Whitcomb et al [2] isolated the first responsible mutation in the trypsinogen gene on the long arm of chromosome seven (7q35).

  8. Malabsorption - Wikipedia

    en.wikipedia.org/wiki/Malabsorption

    Pancreatic enzymes are supplemented orally in pancreatic insufficiency. Dietary modification is important in some conditions: Gluten-free diet in coeliac disease. Lactose avoidance in lactose intolerance. Antibiotic therapy to treat Small Bowel Bacterial overgrowth.

  9. Autoimmune pancreatitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_pancreatitis

    Autoimmune Pancreatitis; Other names: AIP: A. Axial CT image in the pancreatic parenchymal phase shows the typical enlarged, poorly enhancing gland. B. Coronal T2 Weighted MR image demonstrates low signal intensity in the pancreas due to the diffuse fibrosis in the gland.