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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.
IgG4-related mesenteritis (subtypes are: mesenteric panniculitis, mesenteric lipodystrophy and retractile mesenteritis) [44] Sclerosing mesenteritis, systemic nodular panniculitis, liposclerosis mesenteritis, mesenteric Weber–Christian disease, mesenteric lipogranuloma, xanthogranulomatous mesenteritis. [44] Breast: IgG4-related mastitis
Sclerosing bone dysplasia mental retardation; Sclerosing cholangitis; Sclerosing lymphocytic lobulitis; Sclerosing mesenteritis; Sclerosteosis; Sclerotylosis; SCOT deficiency; Scott–Bryant–Graham syndrome; Scott syndrome; Scrapie
This page was last edited on 27 November 2020, at 02:33 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Idiopathic sclerosing mesenteritis; Idiopathic thrombocytopenic purpura; Iduronate 2-sulfatase deficiency; Ie–Im. IFAP syndrome; IgA deficiency; IgA nephropathy;
This page was last edited on 11 December 2016, at 15:54 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Encapsulating peritoneal sclerosis (EPS) is a chronic clinical syndrome with an insidious onset that manifests as chronic undernourishment accompanied by sporadic, acute, or subacute gastrointestinal obstruction symptoms. [1]
This page was last edited on 13 January 2017, at 16:25 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.