A Case of Hemophilia A Diagnosed in a Premature Infant
Journal of the Korean Society of Neonatology
;
: 132-135, 2010.
Artículo
en Coreano
| WPRIM
| ID: wpr-223415
ABSTRACT
Although the majority of abnormal bleeding during the neonatal period results from acquired coagulation disorders, inherited coagulation disorders can also manifest at this time. Hemophilia is the most common of inherited coagulation disorder. Although 40-70% of cases with hemophilia are diagnosed in the neonatal period, few cases have been reported in premature infants. We report a case of a premature infant born at 31 weeks of gestation, diagnosed with hemophilia A by blood coagulation test, coagulation factor assay and study of the F8 gene. The baby was treated with recombinant factor VIII (Recombinate(R), USA) because of repeated seizures and intramuscular hematoma.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Convulsiones
/
Pruebas de Coagulación Sanguínea
/
Factores de Coagulación Sanguínea
/
Factor VIII
/
Recien Nacido Prematuro
/
Trastornos de la Coagulación Sanguínea Heredados
/
Hematoma
/
Hemofilia A
/
Hemorragia
Tipo de estudio:
Estudio diagnóstico
Límite:
Humanos
/
Lactante
/
Recién Nacido
/
Embarazo
Idioma:
Coreano
Revista:
Journal of the Korean Society of Neonatology
Año:
2010
Tipo del documento:
Artículo
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