Korean Circ J.
2002 Jun;32(6):521-525. 10.4070/kcj.2002.32.6.521.
A Case of Hereditary Antithrombin III Deficiency Manifested by Myocardial Infarction and Deep Vein Thrombosis
- Affiliations
-
- 1Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
- KMID: 1858677
- DOI: http://doi.org/10.4070/kcj.2002.32.6.521
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.
- Full Text Links
-
- Actions
-
Cited
- CITED
-
- Close
- Share
-
- Similar articles
-
- A Case of Anti-Thrombin III Deficiency Discovered by Myocardial Infarction
- A Case of Pediatric Unprovoked Deep Vein Thrombosis due to Combined Hereditary Thrombophilia of Antithrombin III and Protein S Deficiency
- A Case of Stasis Dermatitis with Secondary Lipodermatosclerosis in a Patient with Antithrombin III Deficiency
- Cerebral Venous Sinus Thrombosis Associated with Antithrombin III Deficiency: A Case Report
- A case of combined deficiency of antithrombin III and protein C complicated by recurrent venous thrombosis
