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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Appl Clin Genet
Päätekijät: Traivaree, Chanchai, Monsereenusorn, Chalinee, Meekaewkunchorn, Arunotai, Laoyookhong, Premsak, Suwansingh, Saranya, Boonyawat, Boonchai
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove Medical Press 2017
Aiheet:
Case Series
Linkit: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
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