A Case of Hereditary Antithrombin III Deficiency Manifested by Myocardial Infarction and Deep Vein Thrombosis.
10.4070/kcj.2002.32.6.521
- Author:
Ki Young KIM
1
;
Keon Woong MOON
;
Doo Soo JEON
;
Joo Youn CHOI
;
Dae Hyung JEON
;
Jae Wook KIM
;
Jin Sun LEE
;
Min Seok CHOI
;
Gil Hwan LEE
;
Man Young LEE
Author Information
1. Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Myocardial infarction;
Venous thrombosis;
Antithrombin III deficiency
- MeSH:
Antithrombin III Deficiency*;
Antithrombin III*;
Embolism;
Humans;
Myocardial Infarction*;
Pulmonary Embolism;
Thromboembolism;
Venous Thrombosis*
- From:Korean Circulation Journal
2002;32(6):521-525
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Antithrombin III deficiency is an autosomal dominant disorder, which is manifested by recurrent venous thromboembolisms, such as: deep vein thrombosis and/or pulmonary embolism, but arterial embolisms are very rare. We report a case of a patient with hereditary antithrombin III deficiency, manifested by myocardial infarction and deep vein thrombosis.
