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Familial Mediterranean fever in three Japanese patients, and a comparison of the frequency of MEFV gene mutations in Japanese and Mediterranean populations

✍ Scribed by Sugiura, Tomoko; Kawaguchi, Yasushi; Fujikawa, Satoru; Hirano, Yukiko; Igarashi, Toru; Kawamoto, Manabu; Takagi, Kae; Hara, Masako; Kamatani, Naoyuki

Book ID
125807797
Publisher
Springer
Year
2008
Tongue
English
Weight
168 KB
Volume
18
Category
Article
ISSN
1439-7595

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## Abstract ## Objective Familial Mediterranean fever (FMF) is an autosomal‐recessive disorder that is common in Armenian, Turkish, Arab, and Sephardic Jewish populations. Its clinical diagnosis is one of exclusion, with the patients displaying nonspecific symptoms related to serosal inflammation.