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Hemophilia Research Paper

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Hemophilia is a rare disease that affects about 400,000 people worldwide, and occurs mostly in men. In this report I will be talking about symptoms, how you develop it, treatment, testing, living with the disease and more.
Hemophilia is a rare and painful blood disorder where your blood is not able to clot normally. There are two main types of hemophilia. Hemophilia A is a mutation in the gene VIII and type B is a mutation in the gene IX. Type A is four times more common than type B. if a person cuts or suffers internal injuries like a bruise they will bleed longer than a regular person. Also they will have a harder time recovering from the injury. When a person hits any part of their body hard enough the blood will pool inside their body and is very painful. Also when they get cut the blood does not stop without medical help. This disorder is genetic and you can only inherit it. It does not spread like a virus. It is very rare that a genetic mutation will occur and you get the disorder. Some symptoms are you have excessive bleeding from minor cuts, large or deep bruising, swelling in joints, nose bleeds randomly, extreme headache, vomiting, …show more content…
If one of the parents has the disease than the child will most likely have it too. In most cases you get tested a few weeks after birth. Once you get your blood drawn they send it to a special laboratory to get tested. In the test they check your clotting levels and it takes a few weeks to get your results back. There are not very many treatment options. One of them is called replacement therapy. Replacement therapy is where clotting factors are slowly dripped or injected into your vein. This helps because the clotting factors will help you not bleed excessively when you are cut or bruised. This disorder has no environmental factors. The only way you can get it is if you inherit it or from a gene

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