Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population

被引:288
作者
Yilmaz, E [1 ]
Ozen, S
Balci, B
Duzova, A
Topaloglu, R
Besbas, N
Saatci, U
Bakkaloglu, A
Ozguc, M
机构
[1] Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Fac Med, Dept Pediat Rheumatol & Nephrol, Ankara, Turkey
[3] Baskent Univ, Dept Pediat, Ankara, Turkey
[4] Univ Hacettepe, Inst Child Hlth, DNA Cell Bank & Res Labs, TUBITAK, Ankara, Turkey
关键词
FMF; MEFV gene; mutations;
D O I
10.1038/sj.ejhg.5200674
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Familial Mediterranean Fever (FMF) is a recessive disorder characterised by episodes of fever and neutrophil-mediated serozal inflammation. The FMF gene (MEFV) was recently identified and four common mutations characterised. The aim of this study was to determine the carrier rate in the Turkish population and the mutation frequency in the clinically diagnosed FMF patients. We found a high frequency of carriers in the healthy Turkish population (20%). The distribution of the five most common MEFV mutations among healthy individuals (M694V 3%, M6801 5%, V726A 2%, M6941 0% and E148Q 12%) was significantly different (P < 0.005) from that found in patients (M694V 51.55%, M6801 9.22%, V726A 2.88%, M6941 0.44% and E148Q 3.55%).
引用
收藏
页码:553 / 555
页数:3
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