A case of intracranial hemorrhage in a neonate with congenital factor VII deficiency

Congenital factor VII deficiency is a rare autosomal-recessive bleeding disorder. Bleeding manifestations and clinical findings vary widely, ranging from asymptomatic subjects to patients with hemorrhages that may cause significant handicaps. Treatment has traditionally involved factor VII(FVII) rep...

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Detalles Bibliográficos
Autores principales: Lee, Won Seok, Park, Young Sil
Formato: Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004506/
https://www.ncbi.nlm.nih.gov/pubmed/21189963
http://dx.doi.org/10.3345/kjp.2010.53.10.913

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004506/
https://www.ncbi.nlm.nih.gov/pubmed/21189963
http://dx.doi.org/10.3345/kjp.2010.53.10.913

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