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[Genetic risk factors of venous thromboembolism]
Ferda Oner1, Akin Kaya, Ruşina Doğan
1Ankara University Faculty of Medicine, Pulmonary Diseases, Ankara, Turkey. onerferda@hotmail.com
Abstract:
Up to date several hereditary disorders have been identified as prothrombic risk factors. The most common inherited thrombotic disorders include activated protein C resistance (factor V Leiden), prothrombin G20210A mutation, hyperhomocysteinemia, deficiencies of protein C, protein S, antithrombin III, and thrombomodulin. This article focuses on the clinical and the laboratory aspects of some of the inherited venous thrombotic disorders including the factor V Leiden, prothrombin G20210A mutation and protein S deficiency.
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