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- W2327761353 endingPage "144" @default.
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- W2327761353 abstract "Inherited thrombophilia is associated with an increased risk of thrombosis. Classically it consists of protein C and protein S deficiency, activated protein C resistance and antithrombin III deficiency. In pregnancy, in addition to thrombosis, inherited thrombophilia is associated with poor obstetric outcome, including recurrent miscarriage, late fetal loss, abruption and pre-eclampsia. Hyperhomocysteinaemia is a newly recognized cause of familial thrombophilia. It is likely that further causes such as prothrombin gene mutations will be added to the rapidly expanding list. The diagnosis of some forms of genetic thrombophilia must, however, be approached with caution during pregnancy, particularly protein S deficiency and activated protein C resistance." @default.
- W2327761353 created "2016-06-24" @default.
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- W2327761353 date "1998-04-01" @default.
- W2327761353 modified "2023-10-14" @default.
- W2327761353 title "Inherited thrombophilia and pregnancy" @default.
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- W2327761353 doi "https://doi.org/10.1097/00001703-199804000-00010" @default.
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