“Sickle cell trait and haemophilia: a rare association”

In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A. We conclude that it is about a post-circumcision bleeding due to major hemophilia A associate...

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Detalles Bibliográficos
Autores principales: El Maataoui, Hayat, Fahi, Amina, Oukkache, Bouchra
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/PMC5987143/
https://www.ncbi.nlm.nih.gov/pubmed/29875973
http://dx.doi.org/10.11604/pamj.2018.29.92.14551
Descripción
Sumario:In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A. We conclude that it is about a post-circumcision bleeding due to major hemophilia A associated to sickle cell AS, this association was a systematic discovery.

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