Pulmonary Thromboembolism Caused by PROS1 Gene Mutation / 계명의대학술지
Keimyung Medical Journal
;
: 94-98, 2014.
Artículo
en 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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Arginina
/
Embolia Pulmonar
/
Exones
/
Factores de Riesgo
/
Deficiencia de Proteína S
/
Trombofilia
/
Cistina
/
Inmovilización
Tipo de estudio:
Estudio de etiología
/
Factores de riesgo
Límite:
Adulto
/
Humanos
Idioma:
Coreano
Revista:
Keimyung Medical Journal
Año:
2014
Tipo del documento:
Artículo
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