Inherited thrombophilic conditions.

Abstract excerpt

Since 1965, when antithrombin deficiency was identified as the first congenital defect of hemostasis able to increase the risk of thrombosis, we have assisted in a substantial evolution of thrombophilia. From the original monogenic view, it has been demonstrated that thrombosis is a polygenic and complex disorder that involves potentially hundreds of polymorphisms and rare mutations, as well as multiple acquired...

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