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...

Full description

Saved in:
Bibliographic Details
Published in:Appl Clin Genet
Main Authors: Traivaree, Chanchai, Monsereenusorn, Chalinee, Meekaewkunchorn, Arunotai, Laoyookhong, Premsak, Suwansingh, Saranya, Boonyawat, Boonchai
Format: Artigo
Language:Inglês
Published: Dove Medical Press 2017
Subjects:
Case Series
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5484628/
https://ncbi.nlm.nih.gov/pubmed/28684918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S139788
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items