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Hemophilia Research Paper

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Hemophilia A, also known as classic or deficiency hemophilia, is a genetic disorder in which a VIII factor, a clotting protein, is missing or defective. Meaning a person’s blood is not able of clotting normally. This incapacity of blood clotting can occur internally and externally. When bleeding internally, the part in which your are bleeding swells up and the skin turns red or purple, depending on how severe it is. It normally occurs in the joints such as in the knees, elbows, ankles, which can be very painful and lead to crippling and arthritis. Bleeding in areas such as the throat, brain and abdomen can be life-threatening. On the other hand, external bleeding occurs when the skin is cut or opened . It is often triggered by surgery, …show more content…
The type of severity depends on the person’s clotting level. The clotting factor level is shown as a percentage. The normal factor level is 100%. A level between 60% and 200% meets the standard levels. A person with hemophilia has a much lower clotting factor level than the standards. Meaning that it is important to know your clotting factor level so that you know what you are facing and what you are in risk of. A 6% to 25% factor level is considered mild . This type of hemophilia will probably never cause you to bleed on your own nor have joint problems, but you are at the risk to bleed due to a bad injury surgery or shots. The factor level between 1% and 5% is considered moderate. This may cause you to bleed with a slight injury, causing a person probably bleed once a month, often occurring problems in the joints. A factor level less than 1% is considered severe. Severe hemophilia can cause you to bleed without an injury. Meaning that a person may bleed once or twice a month for no apparent reason. This type of severity will most likely with cause a person to bleed internally within the joints. A person's health and physical stability takes a massive roll in the amount of times you

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