Open AccessAssociation of Hereditary Prothrombotic Risk Factors with ST Elevation Myocardial Infarction
Author(s) -
İbrahim Halil Damar,
Recep Eröz
Publication year - 2020
Publication title -
medeniyet medical journal
Language(s) - English
Resource type - Journals
eISSN - 2149-2042
pISSN - 2149-4606
DOI - 10.5222/mmj.2020.67366
Subject(s) - methylenetetrahydrofolate reductase , medicine , myocardial infarction , thrombophilia , cardiology , factor v leiden , protein c deficiency , factor v , prothrombin g20210a , percutaneous coronary intervention , thrombosis , allele , venous thrombosis , gene , genetics , biology
The ST- elevation myocardial infarction (STEMI), a serious health care problem, is commonly a thrombotic complication of coronary artery disease. We compare the STEMI patients and control group in terms of the possible causes of inherited thrombophilia including FactorV Cambridge G1091C, FactorV Leiden G1691A, MTHFRC677T, MTHFR A1298C, FactorII G20210A, Factor XIII (V34L), PAI-1, FGB, ITGB3, APOB, FVHR2, ACE gene variants.