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Pan African Medical Journal

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“Sickle cell trait and haemophilia: a rare association”

Hayat El Maataoui, Amina Fahi, Bouchra Oukkache

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.




AJOL African Journals Online