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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.


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eISSN: 1937-8688