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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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| Publicado en: | Pan Afr Med J |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
The African Field Epidemiology Network
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5579429/ https://ncbi.nlm.nih.gov/pubmed/28904709 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.27.182.12285 |
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