Familial Mediterranean fever (FMF) is an autosomal recessive disease clinically characterized by recurrent short self-limited attacks of fever accompanied by peritonitis, pleurisy, and arthritis and can lead to amyloidosis and renal failure in the longer term. It is prevalent mainly in non-Ashkenazi
β¦ LIBER β¦
Familial Mediterranean Fever and E148Q Pyrin Gene Mutation in Greece
β Scribed by Kostas Konstantopoulos; Alexandra Kanta; Konstantinos Lilakos; George Papanikolaou; Ioannis Meletis
- Book ID
- 111835835
- Publisher
- Carden Jennings Publishing
- Year
- 2005
- Tongue
- English
- Weight
- 51 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0925-5710
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Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by recurrent attacks of fever and serositis, common in populations of Armenian, Arab, Sephardic Jewish and Turkish origin. Early diagnosis is crucial to start colchicine therapy that prevents the occurrence of attack