Hemophilia, The Most Common Form Essay

1309 Words Nov 15th, 2016 6 Pages
Hemophilia is a genetic blood disease, which is symbolized by the importance of blood to clot, or compact even from inconsequential damage. Blood clotting and sudden gene mutation factor in the development of this disease. This disease is generated by an inadequacy of blood multifaceted called factors Therefore, with the nonappearance of factors, the blood clotting process is continued. There are two different types of Hemophilia, Hemophilia A and Hemophilia B. for example. Hemophilia A, the most common form is caused by the lack of factor VIII. Whereas, in Hemophilia B (also known as Christmas disease), factor IX is absent. This disease develops and affects people from their birth. This disease is also developed and transmitted to children from their parents at birth. Because of its genetic makeup, Hemophilia in female is a rare occurrence and only happens if both X chromosomes are affected, one of their X-chromosomes is a carrier. But Hemophilia affects males after inheriting an affected X-chromosomes with mutation.
Only for one third of the time, Hemophilia begins by unplanned gene alteration with no family background or history. This is how females can be bothered by Hemophilia. Inheritance is controlled by a recessive sex-linked factor carried by the mother on the X-chromosome. There is a high chance that the sons of a female carrier will have Hemophilia. There also is a fifty percent chance that the daughters of a female carrier will be carriers of Hemophilia. In…

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