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"Sickle cell trait and haemophilia: a rare association"
Hayat El Maataoui1,2, Amina Fahi1,2, Bouchra Oukkache1,2
1Ibn Rochd Teaching Hospital Hematology Laboratory Casablanca, Maroc.
The Pan African Medical Journal
|June 8, 2018
Abstract:
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.