Pulmonary Thromboembolism Caused by PROS1 Gene Mutation / 계명의대학술지
Keimyung Medical Journal
;
: 94-98, 2014.
Artigo
em Coreano
| WPRIM
| ID: wpr-191854
ABSTRACT
Pulmonary embolism (PE) is a serious clinical problem in patients with acquired risk factor such as cancer, immobilization, recent trauma and surgery. However PE may occur in hereditary thrombophilia like protein S deficiency which is caused by PROS1 gene mutation. The author reports a case of pulmonary embolism in a 33-year-old man with protein S deficiency and PROS1 gene mutation. Genetic analysis of the patient showed mutation 1063C→T in exon 10 of PROS1 gene, resulting in a substitution of arginine by cystine at position 355 (R355C).
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Arginina
/
Embolia Pulmonar
/
Éxons
/
Fatores de Risco
/
Deficiência de Proteína S
/
Trombofilia
/
Cistina
/
Imobilização
Tipo de estudo:
Estudo de etiologia
/
Fatores de risco
Limite:
Adulto
/
Humanos
Idioma:
Coreano
Revista:
Keimyung Medical Journal
Ano de publicação:
2014
Tipo de documento:
Artigo
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