Déficit congénital en facteur VII de coagulation: à propos de deux cas familiaux

Factor VII deficiency is rare, with an estimated prevalence rate of 1/1,000,000. It is transmitted as an autosomal recessive trait. It can cause simple nosebleeds up to cerebral hemorrhage. Our study aims to focus on the clinical features and the importance of screening in patients with this rare de...

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Detalles Bibliográficos
Autores principales: Benajiba, Noufissa, Ayyad, Anass, Aabdi, Chourouk, Amrani, Rim, Rkain, Maria, Benajiba, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488256/
https://www.ncbi.nlm.nih.gov/pubmed/31065316
http://dx.doi.org/10.11604/pamj.2018.31.156.6123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488256/
https://www.ncbi.nlm.nih.gov/pubmed/31065316
http://dx.doi.org/10.11604/pamj.2018.31.156.6123

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