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العنوان
Evaluation of the relation between factor V leiden (G1691A), prothrombin (G20210A) gene mutations and idiopathic recurrent pregnancy loss =
المؤلف
Abdel Razek, Yomna Moheb Mansour.
هيئة الاعداد
باحث / Yomna Moheb Mansour Abdel Razek
مشرف / Amal Kotb Behery
مشرف / Nargues Mahmoud Aly
مشرف / Muhammad Fawzy
الموضوع
Genatics.
تاريخ النشر
2013.
عدد الصفحات
102 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
علم الوراثة (السريرية)
تاريخ الإجازة
11/6/2014
مكان الإجازة
جامعة الاسكندريه - معهد البحوث الطبية - Genatics
الفهرس
Only 14 pages are availabe for public view

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Abstract

Evaluation Of The Relation Between Factor V Leiden,
Prothrombin Gene Mutation And Recurrent pregnancy loss
Recurrent pregnancy loss is defined as two or three consecutive pregnancy losses, causes of RPL includes genetic, uterine, hormonal and immunological, now inherited thrombophilia is suggested as a possible cause of RPL. Thrombophilia is defined as increased tendency of blood to clot increasing risk for thrombosis . The aim of the study was to evaluate the role of FVL , prothrombin gene mutation the most common mutations responsible for inherited thrombophilia in RPL, this will allow couples at high risk for RPL due to these two mutations to receive proper genetic counseling ,treatment and improve pregnancy outcome.
the study was carried out on 56 cases had at least two consecutive losses
after exclusion of all known causes of RPL and control group of 48 women
had at least one child without any complications in pregnancy, there was
increased prevalence of both mutations in cases than control but to a non
significant level, a statistically significant increase was reported in cases
had abortion in second trimester compared to cases had abortion in first
trimester.