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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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Main Authors: | , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
The Korean Pediatric Society
2010
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3004506/ https://ncbi.nlm.nih.gov/pubmed/21189963 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2010.53.10.913 |
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