Aim: Familial Mediterranean fever is an autosomal recessive disease affecting primarily populations surrounding the Mediterranean basin. The aim of this study was to find the distribution of MEFV gene mutations in a group of Egyptian patients with FMF and to evaluate any predictive genotype-phenotype correlation in this group of patients. Materials and Methods: The study included 112 patients (59 males and 53 females). Sequencing of the exon 10, exon 3, and exon 5 and PCR/RFLP analysis of E148Q and R202Q mutations of exon 2 of the MEFV gene were performed for all the patients according to a previously described technique. Results: Mutations in the MEFV gene were identified in 63 patients (56.25%). The most common mutation was M694I, which was detected in 9.8%, followed by V726A in 7.1%, E148Q in 5.8%, R202Q in 4.9%, M694V in 4.5%, M680I(G/C) in 3.1%, M680I(G/A) in 3.1%, and P706 in 2.6% of studied chromosomes. Conclusions: The mutation spectrum in Egyptian patients with FMF is heterogeneous. R202Q and P706 might be disease-causing mutations and should be further investigated in more patients in different populations.
Familial Mediterranean fever (FMF), MEFV gene, Egypt
ÖZTÜRK, AYŞENUR; ELSOBKY, EZZAT; ELSAYED, SOLAF M.; ALHODHOD, MOSTAFA; and AKAR, NEJAT
"Mutational Analysis of the MEFV Gene in Egyptian Patients with Familial Mediterranean Fever,"
Turkish Journal of Medical Sciences: Vol. 39:
2, Article 12.
Available at: https://journals.tubitak.gov.tr/medical/vol39/iss2/12