International Journal of Genetics and Genomics
Volume 3, Issue 5, October 2015, Pages: 50-52
Received: Aug. 26, 2015;
Accepted: Sep. 6, 2015;
Published: Sep. 14, 2015
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Mohammed J. Ashour, Department of Medical Laboratory Sciences, Faculty of Health Sciences, the Islamic University of Gaza, Gaza, Palestine
Fadel A. Sharif, Department of Medical Laboratory Sciences, Faculty of Health Sciences, the Islamic University of Gaza, Gaza, Palestine
Familial Mediterranean fever (FMF) is an autosomal recessive inflammatory disorder caused by mutations in the MEFV gene that encodes the pyrin protein. The disease is relatively common among people originating from the Mediterranean areas. The aim of this study was to determine the common MEFV gene mutations in 270 Palestinian patients diagnosed with FMF. The patients were screened for four common MEFV gene mutations namely, p.M694V, p.M694I, p.V726A, and p.E148Q using allele-specific polymerase chain reaction (AS-PCR). The results revealed that around 22% of the patients harbored two MEFV mutations, with the compound heterozygous forms being more prevalent than the homozygous ones. The most frequently encountered mutant allele was p.M694V which existed in around 12% of the tested chromosomes. The p.M694I, p.V226A and p.E148Q mutations were observed in around 9, 9 and 7% of the tested chromosomes, respectively. In about 29% of the patients only one mutant allele could be detected and around 49% of the patients did not show any of the investigated mutations. In conclusion, the four tested MEFV gene mutations have a significant contribution to FMF in the Palestinian population of Gaza strip. Screening for those mutations should be offered to FMF patients to confirm diagnosis and effect timely treatment. Further mutations analysis the MEFV gene should be conducted in this population in order to document additional MEFV mutations.
Mohammed J. Ashour,
Fadel A. Sharif,
Common MEFV Mutations in Palestinian Patients with Familial Mediterranean Fever, International Journal of Genetics and Genomics.
Vol. 3, No. 5,
2015, pp. 50-52.
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