Genetic risk factors of venous thromboembolism Venöz Tromboembolizmde Kalitsal Risk Faktörleri.

Oner F., KAYA A., Dogan R., Numanoglu N.

Tüberküloz ve toraks, vol.51, no.1, pp.60-69, 2003 (SCI-Expanded, Scopus, TRDizin) identifier identifier

  • Publication Type: Article / Review
  • Volume: 51 Issue: 1
  • Publication Date: 2003
  • Journal Name: Tüberküloz ve toraks
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.60-69
  • Ankara University Affiliated: Yes

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.