Abstract:In 81 women referred for diagnosis-therapy of atherothrombotic and endocrine disorders, and found to be heterozygous (n = 49) or homozygous (n = 3) for the G1691A Factor V Leiden mutation (FV), or heterozygous (n = 29) for the G20210A prothrombin gene mutation (PTG), and having ≥ 1 pregnancy, our specific aim was to assess relationships of familial thrombophilia to previous pregnancy outcomes. The 52 women with FV (1 black, 43 white, 8 other, 47 ± 13 years old) had 164 pregnancies with 114 live births (70%) an… Show more
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