A Case of Hereditary Antithrombin III Deficiency Manifested by Myocardial Infarction and Deep Vein Thrombosis
Korean Circulation Journal
; : 521-525, 2002.
Article
em Ko
| WPRIM
| ID: wpr-65740
Biblioteca responsável:
WPRO
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.
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Texto completo:
1
Índice:
WPRIM
Assunto principal:
Embolia Pulmonar
/
Tromboembolia
/
Antitrombina III
/
Trombose Venosa
/
Deficiência de Antitrombina III
/
Embolia
/
Infarto do Miocárdio
Limite:
Humans
Idioma:
Ko
Revista:
Korean Circulation Journal
Ano de publicação:
2002
Tipo de documento:
Article