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Idiopathic sclerosing mesenteritis (ISM) is a rare disease of the small intestine, characterized by chronic inflammation and eventual fibrosis of the mesentery. [1] It has also been called mesenteric lipodystrophy, or retractile mesenteritis.
Idiopathic sclerosing mesenteritis; Idiopathic thrombocytopenic purpura; Iduronate 2-sulfatase deficiency; Ie–Im. IFAP syndrome; IgA deficiency; IgA nephropathy;
IgG4-related disease (IgG4-RD), formerly known as IgG4-related systemic disease, is a chronic inflammatory condition characterized by tissue infiltration with lymphocytes and IgG4-secreting plasma cells, various degrees of fibrosis (scarring) and a usually prompt response to oral steroids.
Schaap–Taylor–Baraitser syndrome; Schaefer–Stein–Oshman syndrome; Schamberg's disease pigmentation disorder; Schamberg's disease; Scheie syndrome
In the human embryo, the vitelline duct, also known as the vitellointestinal duct, [1] the yolk stalk, [1] the omphaloenteric duct, [1] or the omphalomesenteric duct, [1] is a long narrow tube that joins the yolk sac to the midgut lumen of the developing fetus. [2]
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For the most common cause, peritoneal carcinomatosis, omental caking is associated with a wide variety of symptoms. Ascites and intestinal peristalsis is known to have an effect on how diffusely the cancer cells are spread throughout the abdomen.
Retroperitoneal fibrosis or Ormond's disease is a disease featuring the proliferation of fibrous tissue in the retroperitoneum, the compartment of the body containing the kidneys, aorta, renal tract, and various other structures.