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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...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Pediatric Society
2010
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| 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 |