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What is Hemophilia A?

Hemophilia A is one type of hemophilia. Hemophilia is an inherited disease that prevents the blood from clotting properly. People with hemophilia have a deficiency of a blood protein, also called a "clotting factor," that is necessary to clot the blood and stop bleeding. Originally, hemophilia was thought to be one disease condition. In the 1950s, two separate forms of hemophilia were discovered: hemophilia A and hemophilia B.1,2

People with hemophilia A, also called "classic hemophilia," have a deficiency in clotting factor VIII. In some cases, especially in severe hemophilia, the individual simply has low levels of factor VIII. Typically, however, factor VIII is present but is defective (inactive) in some way. Hemophilia A is the most common form of hemophilia, occurring in about 80% of all cases.1

Click Here For More Hemophilia A Information(http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowSection&rid=gnd.section.95)

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