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자료유형
학술저널
저자정보
Han, Sung Hee (Division of Biotechnology, Bio-Core Co. Ltd.) Seo, Jung Jae (Department of Obstetrics and Gynecology, Women's I Hospital) Kim, Eun Seol (Department of Obstetrics and Gynecology, Women's I Hospital) Ryu, Jae Song (Division of Biotechnology, Bio-Core Co. Ltd.) Hong, Seong Hyeon (Division of Biotechnology, Bio-Core Co. Ltd.) Hwang, Seung Yong (Division of Biotechnology, Bio-Core Co. Ltd.)
저널정보
대한의학유전학회 Journal of genetic medicine Journal of genetic medicine 제16권 제1호
발행연도
2019.1
수록면
23 - 26 (4page)

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Thrombophilia refers to inherited or acquired hemostatic disorders that result in a predisposition to blood clot formation. When combined with the hypercoagulable state that is characteristic of pregnancy, there is an increased risk of severe and recurrent pregnancy complications. Activated protein C resistance caused by factor V Leiden (FVL) mutation is known to be the most common cause of inherited thrombophilia in Caucasian population. FVL mutation has been related to pregnancy complications associated with hypercoagulation, e.g. miscarriage, intrauterine fetal demise, placental abruption, and intrauterine growth retardation. Although the FVL mutation is easily detected using molecular DNA techniques, patients who are heterozygous for this disorder often remain asymptomatic until they develop a concurrent prothrombotic condition. Because there are potentially serious effects of FVL mutation for pregnancy, and because effective treatment strategies exist, early detection and treatment of this condition might be considered.

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