Déficit congénital en facteur V: à propos d’un cas

Factor V congenital deficiency is a rare coagulation disorder initially described by Owren in 1947 and known as para hemophilia. It is transmitted through autosomal-recessive inheritance and homozygous cases are usually symptomatic. Factor V is an essential cofactor in the conversion of prothrombin...

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Detalles Bibliográficos
Autores principales: Boujrad, Saloua, El Hasbaoui, Brahim, Echahdi, Hanae, Malih, Mohamed, Agadr, Aomar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579429/
https://www.ncbi.nlm.nih.gov/pubmed/28904709
http://dx.doi.org/10.11604/pamj.2017.27.182.12285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579429/
https://www.ncbi.nlm.nih.gov/pubmed/28904709
http://dx.doi.org/10.11604/pamj.2017.27.182.12285

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