Familial Mediterranean Fever in the World

被引:324
作者
Ben-Chetrit, Eldad [1 ]
Touitou, Isabelle [2 ]
机构
[1] Hadassah Hebrew Univ, Med Ctr, Familial Mediterranean Fever Ctr, Jerusalem, Israel
[2] CHU Montpellier, Unite Med Malad Autoinflammatoires, Hop A de Villeneuve, Montpellier, France
关键词
GENOTYPE-PHENOTYPE CORRELATION; MEFV MUTATIONS; POPULATION-GENETICS; FMF; COLCHICINE; AMYLOIDOSIS; CHILDREN; RESISTANT; DISEASE; POLYSEROSITIS;
D O I
10.1002/art.24458
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The above overview shows that FMF is not restricted to Mediterranean countries, and the lack of diagnosis in other areas of the world is probably due to a lack of awareness of this fascinating disease. Based on the carrier states of MEFV mutations, FMF is expected to be found in many other countries and it may well be that such patients have either mild disease according to the kind of mutations they carry or the environmental factors, or that they were mistakenly diagnosed as having another disease such as BD, systemic lupus erythematosus, palindromic rheumatism, or rheumatic fever, diseases whose clinical features resemble FMF. We hope that the present review will raise the awareness of physicians regarding this disease so that patients can obtain the correct diagnosis and receive the appropriate treatment.
引用
收藏
页码:1447 / 1453
页数:7
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