Combined Factor V and Factor VIII Deficiency among Non-Ashkenazi Jews

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Abstract
Combined factor V and factor VIII deficiency is a well-documented hereditary bleeding disorder that has so far been reported in 21 families.1 , 2 The study of this disorder is of great interest, since the normal function of factor V and factor VIII is controlled by separate genes — a fact that can be inferred from the existence of hemophilia A and von Willebrand's disease (factor VIII deficiencies), on the one hand, and of parahemophilia (a factor V deficiency), on the other. Recently, a mechanism for the combined factor V and factor VIII deficiency has been proposed by Marlar and Griffin,3 who . . .