Hemophilias. Hemophilia is a bleeding disorder, usually inherited with an x-linked recessive inheritance pattern, which results from the deficiency of a coagulation factor. Hemophilia a results from the deficiency of clotting factor viii. Hemophilia b results from the deficiency of clotting factor ix. Acquired hemophilia is a separate noninherited condition, rarer than congenital hemophilia, autoimmune.
Bleeding disorder. Hemophilia a is due to the absence of clotting factor viii (most common) hemophilia b is due to the absence of clotting factor ix (less common).
Deficiency factor 8. The difference is that hemophilia a is due to a deficiency of factor 8 (viii), while hemophilia b is from a deficiency of factor 9 (ix). Both are sex-linked recessive, and both have similar lab findings of a normal pt and high ptt. The treatment of each is replacement of the respective factors. Hemopnilia a gets factor 8 while hemophilia b get factor 9 in concentrates or fresh frozen plasma. Read more...