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Publication year
2005Source
Best Practice & Research in Clinical Gastroenterology, 19, 2, (2005), pp. 199-213ISSN
Publication type
Article / Letter to editor
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Organization
Internal Medicine
Gastroenterology
Journal title
Best Practice & Research in Clinical Gastroenterology
Volume
vol. 19
Issue
iss. 2
Page start
p. 199
Page end
p. 213
Subject
EBP 3: Effective Primary Care and Public Health; IGMD 2: Molecular gastro-enterology and hepatology; N4i 1: Pathogenesis and modulation of inflammation; N4i 2: Invasive mycoses and compromised host; NCMLS 1: Infection and autoimmunity; NCMLS 5: Membrane transport and intracellular motility; UMCN 4.1: Microbial pathogenesis and host defense; UMCN 5.1: Genetic defects of metabolismAbstract
Familial Mediterranean fever is a hereditary syndrome characterised by recurrent episodes of fever and serositis, resulting in pain in the abdomen, chest, joints and muscles. It is primarily diagnosed in people of Jewish, Arabic, Turkish or Armenian ancestry and is caused by mutations in the gene encoding for pyrin. Abdominal FMF attacks resemble the clinical presentation of 'acute abdomen', with severe abdominal pain and rigidity, but in FMF symptoms always resolve spontaneously. It is important to distinguish these regular pain episodes from small bowel obstruction due to adhesions to prevent life-threatening bowel strangulation. In most cases, colchicine will prevent new painful attacks. This seminar also discusses other causes of abdominal pain in FMF patients.
This item appears in the following Collection(s)
- Academic publications [243984]
- Electronic publications [130695]
- Faculty of Medical Sciences [92811]
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