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

305Citations
Citations of this article
85Readers
Mendeley users who have this article in their library.

Abstract

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%).

Author supplied keywords

Cite

CITATION STYLE

APA

Yilmaz, E., Ozen, S., Balci, B., Duzova, A., Topaloglu, R., Besbas, N., … Ozguc, M. (2001). Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population. European Journal of Human Genetics, 9(7), 553–555. https://doi.org/10.1038/sj.ejhg.5200674

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free