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Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children
Congenital factor VII (FVII) deficiency is a rare inherited coagulopathy. The clinical manifestations and clinical findings vary widely, ranging from asymptomatic to life-threatening bleeding, including intracranial hemorrhage (ICH), with prolonged prothrombin time, normal partial thromboplastin tim...
Autores principales: | Traivaree, Chanchai, Monsereenusorn, Chalinee, Meekaewkunchorn, Arunotai, Laoyookhong, Premsak, Suwansingh, Saranya, Boonyawat, Boonchai |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484628/ https://www.ncbi.nlm.nih.gov/pubmed/28684918 http://dx.doi.org/10.2147/TACG.S139788 |
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