Journal of Blood Research

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Articles On Hemophilia

Hemophilia may be a bleeding disorder that impairs the body's ability to regulate coagulation or blood coagulation i.e. during which the blood doesn't clot normally. Hemophilia may be a hereditary disorder that's passed from parents to offsprings. Hemophilia is assessed into two type’s hemophilia A and hemophilia B . hemophilia A may be a dditionally referred to as antihemophilic factor (FVIII) deficiency or classic hemophilia which is a recessive X-linked genetic disease involving a scarcity of functional coagulation factor VIII and represents 80% of hemophilic cases. hemophilia B also called Christmas factor (FIX) deficiency or hemophilia B which may be a recessive X-linked genetic disease involving a scarcity of functional coagulation factor IX. It comprises approximately 20% of hemophilic cases. Journal of Blood Disorders & transfusion publishes articles associated with hemophilia which are subjected to rigorous

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