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Original Article

Double versus single thrombophilias during pregnancy

, , , , , & show all
Pages 2590-2593 | Received 10 Mar 2017, Accepted 28 Jun 2017, Published online: 16 Jul 2017

References

  • ACOG Practice Bulletin No. 138: Inherited thrombophilias in pregnancy. Obstet Gynecol. 2013;122(3):706–717.
  • Rey E, Kahn SR, David M, et al. Thrombophilic disorders and fetal loss: a meta-analysis. Lancet. 2003;361(9361):901–908.
  • Gerhardt A, Scharf RE, Beckmann MW, et al. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium. N Engl J Med. 2000;342(6):374–380.
  • Davenport WB, Kutteh WH. Inherited thrombophilias and adverse pregnancy outcomes: a review of screening patterns and recommendations. Obstet Gynecol Clin North Am. 2014;41(1):133–144.
  • Preston FE, Rosendaal FR, Walker ID, et al. Increased fetal loss in women with heritable thrombophilia. Lancet. 1996;348(9032):913–916.
  • Larciprete G, Rossi F, Deaibess T, et al. Double inherited thrombophilias and adverse pregnancy outcomes: fashion or science? J Obstet Gynaecol Res. 2010;36(5):996–1002.
  • Hundsdoerfer P, Vetter B, Stöver B, et al. Homozygous and double heterozygous factor V Leiden and Factor II G20210A genotypes predispose infants to thromboembolism but are not associated with an increase of foetal loss. Thromb Haemost. 2003;90:628–635.

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