Tab Application Banner
  • Users Online: 311
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
Year : 2014  |  Volume : 9  |  Issue : 1  |  Page : 4-8

Familial Mediterranean fever in the Iranian population: MEFV mutations in different ethnic groups

1 Department of Genetic, Faculty of Biology, Shahid Beheshti University, Tehran, Iran
2 Department of Pediatrics, Kamkar Hospital, Qom University of Medical Sciences and Health Services, Qom, Iran
3 Ahwaz Jundishapur University of Medical Sciences and Health Services, Ahwaz, Iran
4 Hazrat-e-Rasoul Hospital, Tehran University of Medical Sciences and Health Services, Tehran, Iran

Correspondence Address:
Maryam Hosseini
Department of Genetic, Faculty of Biology, Shahid Beheshti University, Tehran
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.1016/j.injr.2013.10.002

Rights and Permissions

Background and aims: Familial Mediterranean Fever (FMF) is an ethnically restricted genetic disease, found commonly among Mediterranean population, as well as Armenians, Turks, Arabs and Jews. The disease is caused by mutations in the MEFV gene, encoding the Pyrin protein. The aim of this study was to determine the mutation frequency in the clinically diagnosed FMF patients and the carrier rate among healthy first-degree relatives of patients from Iran. Methods: 59 patients (<17 years old) with clinical diagnosis of FMF in the absence of colchicine and 82 healthy family members, in three different ethnic groups were screened for the 5 most common MEFV mutations (M694V, M694I, M680I, V726A and E148Q). Results: The mean age of patients (27 females: 32 males) was 7.8 ΁ 3.23. Fever (94.9%) and abdominal pain (77.9%) was the most common clinical finding. Allele frequencies were different among different ethnic groups of Iranian population (p ¼ 0.03). The most frequent mutation was M694V (29.6%) followed by M694I (8%), M680I (15%), V726A (16%) and E148Q (8%): homozygous (18.6%), compound heterozygous (52.5%) and simple heterozygous (16.9%). we could not detect any mutations in 16.95% of our patients. 9 (18%) healthy rel- atives were detected to have mutations of FMF. Conclusions: M694V was the most common MEFV mutation in various ethnic groups of Iranian patients.

Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)

 Article Access Statistics
    PDF Downloaded368    
    Comments [Add]    
    Cited by others 2    

Recommend this journal