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Revision as of 18:41, 20 July 2016

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Asiri Ediriwickrema, M.D., M.H.S. [2]

Overview

Common risk factors in the development of acquired thrombophlias are trauma, surgery, immobility, pregnancy, estrogen-replacement therapy, and age. Common risk factors in the development of inherited thrombophilias are genetic mutations in Factor V Leiden and Prothrombin G20210A.

Risk Factors

Common risk factors in the development of acquired thrombophlias include:

Common risk factors in the development of inherited thrombophilias are genetic mutations in Factor V Leiden and Prothrombon G20210A.[1][2][3]

Please see thrombophilia classification for a list conditions associated with acquired thrombophilias, and to the page on causes of thrombophilia by organ system

References

  1. Cohoon KP, Heit JA (2014). "Inherited and secondary thrombophilia". Circulation. 129 (2): 254–7. doi:10.1161/CIRCULATIONAHA.113.001943. PMC 3979345. PMID 24421360.
  2. Seligsohn U, Lubetsky A (2001). "Genetic susceptibility to venous thrombosis". N Engl J Med. 344 (16): 1222–31. doi:10.1056/NEJM200104193441607. PMID 11309638.
  3. Middeldorp S (2011). "Evidence-based approach to thrombophilia testing". J Thromb Thrombolysis. 31 (3): 275–81. doi:10.1007/s11239-011-0572-y. PMC 3056012. PMID 21340752.

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