A Case of Hereditary Antithrombin III Deficiency Manifested by Myocardial Infarction and Deep Vein Thrombosis
Korean Circulation Journal
;
: 521-525, 2002.
Article
in Korean
| WPRIM
| ID: wpr-65740
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:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pulmonary Embolism
/
Thromboembolism
/
Antithrombin III
/
Venous Thrombosis
/
Antithrombin III Deficiency
/
Embolism
/
Myocardial Infarction
Limits:
Humans
Language:
Korean
Journal:
Korean Circulation Journal
Year:
2002
Type:
Article
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