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...

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Detalles Bibliográficos
Autores principales: Traivaree, Chanchai, Monsereenusorn, Chalinee, Meekaewkunchorn, Arunotai, Laoyookhong, Premsak, Suwansingh, Saranya, Boonyawat, Boonchai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Case Series
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

Internet

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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