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July 04, 2009  
EDUCATION CENTER: Clinical Overview

Clinical Overview
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  • Hemophilia

    Clinical Overview

    Reviewed by Dr. Clement J. Cheng

    Hemophilia is a hereditary blood coagulation disorder, caused by a deficiency of certain clotting factors. Hemophiliacs, or people who have hemophilia, have difficulty having their blood clot once they are bleeding. Hemophilia is potentially a very serious disorder that affects men more often than women.

    There are two types of hemophilia: Hemophilia A and B. Hemophilia A is the most common of these disorders and is the result of a deficiency of clotting factor VIII. The disorder is an inherited genetic disorder. Hemophilia A is a sex-linked recessive trait, with the defective gene located on the X chromosome. As a result, women are the carriers of hemophilia. Half of the male offspring of female carriers have the disease and half of their female offspring are carriers. All female children of a male hemophiliac are carriers of the trait.


    Last updated: Jan-01-00

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