Hereditary coagulation factor X deficiency.
Indian Pediatr
;
2005 Dec; 42(12): 1240-2
Artículo
en Inglés
| IMSEAR
| ID: sea-11059
ABSTRACT
Stuart Prower factor (Factor X) deficiency is a rare hereditary autosomal recessive coagulation disorder. We have come across three cases in the course of last 20 years at our institute. These patients presented with prolonged bleeding after minor trauma, epistaxis, subcutaneous bluish black nodules and two of them presented with history of consanguinity in parents. Hematological findings in correlation with clinical manifestations revealed severe factor X deficiency.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Pruebas de Coagulación Sanguínea
/
Humanos
/
Masculino
/
Preescolar
/
Adolescente
/
Deficiencia del Factor X
/
India
/
Lactante
País/Región como asunto:
Asia
Idioma:
Inglés
Revista:
Indian Pediatr
Año:
2005
Tipo del documento:
Artículo
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