Clinical problems and surgical interventions in inherited factor VII deficiency

AIM: Factor VII deficiency is one of the hereditary coagulation disorders that has autosomal reccessive inheritance and is observed relatively frequently (1/500 000). It is clinically heterogeneous, and may be asymptomatic or lead to life-threatening bleeding. Thus, there is no correlation between F...

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Detalles Bibliográficos
Autores principales: Şenol, Başak Koç, Zülfikar, Bülent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2020
Materias:
Original Article / Özgün Araştırma
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344127/
https://www.ncbi.nlm.nih.gov/pubmed/32684764
http://dx.doi.org/10.14744/TurkPediatriArs.2020.79069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344127/
https://www.ncbi.nlm.nih.gov/pubmed/32684764
http://dx.doi.org/10.14744/TurkPediatriArs.2020.79069

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