Purpose: To assess the relationship of factor V leiden G1691A mutation as a risk factor for repeated pregnancy loss. The focus has been on factor V leiden G1691A mutation that may predispose women to microthrombosis during the stages of embryo implantation and placentation. Methods: A total of 70 women with recurrent pregnancy loss, mean age 31.1±4.2 years, were involved in the study. As a control group, 70 women [mean age 32.2±3.3 years with at least two live-born child and no history of abortion were included. We used real-time polymerase chain reaction (PCR) to determine the frequencies of factor V leiden G1691A genotype. Results: The frequency of heterozygotes for factor V leiden G1691A was significantly higher in women with repeated pregnancy loss compared to women without abortion (p = 0.0001). Conclusion: In summary we found an association of factor V leiden G1691A mutation with recurrent pregnancy loss .We recommend for factor V leiden G1691A screening in cases with repeated pregnancy loss so they can start anticoagulant therapy more earlier.
Ezz Eldein, A., El Sharkawy, E., Salah, K., Ghobrial, A., & Higazi, A. (2020). Association of Factor V Leiden G1691a in Women Suffering Repeated Abortions. Minia Journal of Medical Research, 31(1), 36-42. doi: 10.21608/mjmr.2022.221387
MLA
Asmaa kh. Ezz Eldein; Esmat A. El Sharkawy; Khalid M. Salah; Ayman G. Ghobrial; Aliaa M. Ali Higazi. "Association of Factor V Leiden G1691a in Women Suffering Repeated Abortions". Minia Journal of Medical Research, 31, 1, 2020, 36-42. doi: 10.21608/mjmr.2022.221387
HARVARD
Ezz Eldein, A., El Sharkawy, E., Salah, K., Ghobrial, A., Higazi, A. (2020). 'Association of Factor V Leiden G1691a in Women Suffering Repeated Abortions', Minia Journal of Medical Research, 31(1), pp. 36-42. doi: 10.21608/mjmr.2022.221387
VANCOUVER
Ezz Eldein, A., El Sharkawy, E., Salah, K., Ghobrial, A., Higazi, A. Association of Factor V Leiden G1691a in Women Suffering Repeated Abortions. Minia Journal of Medical Research, 2020; 31(1): 36-42. doi: 10.21608/mjmr.2022.221387