中国医学科学院学报2012，Vol.34Issue(6)：645-648,4.DOI:10.3881/j.issn.1000-503X.2012.06.022
遗传性抗凝血酶缺乏合并高同型半胱氨酸血症与静脉血栓栓塞性疾病
Hereditary Antithrombin Deficiency and Hyperhomocysteinemia in Venous Thromboembolic Disease
郑西希 1邴钟兴 1刘暴1
作者信息
- 1. 中国医学科学院北京协和医学院北京协和医院血管外科,北京100730
- 折叠
摘要
Abstract
Hypercoagulability state is the result of the interplay of genetic predisposition and risk factors. Many key enzymes and reactions in coagulation and anti-coagulation system are involved. Hereditary antithrombin deficiency is one of the major risk factors of venous thromboembolic disease (VTE) , whereas hyperhomocysteinemia may also play a role. This article reviews the recent researches on the contributions of these two factors to VTE.关键词
遗传性抗凝血酶缺乏/高同型半胱氨酸血症/静脉血栓栓塞性疾病Key words
hereditary antithrombin deficiency/ hyperhomocysteinemia/ venous thromboembolic disease分类
医药卫生引用本文复制引用
郑西希,邴钟兴,刘暴..遗传性抗凝血酶缺乏合并高同型半胱氨酸血症与静脉血栓栓塞性疾病[J].中国医学科学院学报,2012,34(6):645-648,4.
