## 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.
✦ LIBER ✦
Familial Mediterranean fever: High gene frequency among the non-Ashkenazic and ashkenazic Jewish populations in Israel
✍ Scribed by Daniels, M. ;Shohat, T. ;Brenner-Ullman, A. ;Shohat, M.
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 397 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Familial Mediterranean fever among patie
✍
Cécile Cazeneuve; Zaruhi Hovannesyan; David Geneviève; Hasmik Hayrapetyan; Stéph
📂
Article
📅
2003
🏛
John Wiley and Sons
🌐
English
⚖ 101 KB
👁 2 views
Diagnostic value of MEFV gene analysis i
✍
Isabelle Touitou
📂
Article
📅
2004
🏛
John Wiley and Sons
🌐
English
⚖ 87 KB
👁 2 views
In their recent article, Cazeneuve et al investigated the diagnostic value of MEFV gene analysis in populations classically affected with familial Mediterranean fever (FMF) (1). They concluded that a search for very few mutations is highly sensitive in the molecular diagnosis of MEFV-related FMF.