Highlights the increasing recognition of various thrombophilic disorders as causes of venous thromboembolism in maternal-fetal medicine.
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May prompt thrombophilia evaluation in maternal VTE; leaves open prospective validation before practice change.
Twenty years ago we did not have a problem with thrombophilia as a cause of venous thromboembolism in pregnant and postpartum women, or rather, we did not know we had a problem. The only known major thrombophilic disorder was deficiency of antithrombin, and it was found only rarely in such women. Recently, there has been a dramatic increase in the number of identifiable causes of thrombophilia. They include, in addition to antithrombin deficiency, protein C and protein S deficiencies, factor V Leiden, the G20210A mutation of the prothrombin gene, and homozygosity for the thermolabile variant of methylenetetrahydrofolate reductase (C677T MTHFR), . . .
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Ian A. Greer (2000) studied this question.
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