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HEMOPHILIA.
Hemophilia is an inherited disease, which prevents the body from clotting blood. People with hemophilia have trouble clotting blood is because they have a low level of protein called factors. Hemophilia is separated into two categories Hemophilia A, and Hemophilia B. The difference between the two is only that it has different amounts of factors. In the US only 400,000 people have hemophilia. Out of the 400,000 people who have this disease 400 babies are born with this disease. What causes hemophilia is that this inherited disease is passed on the X chromosome. Although a male has an XY chromosome a male will never pass this disease on to there sons, but there is a chance that they would to there daughters. Some symptoms that u would have if u had hemophilia would be uncontrollable bleeding, bruises from small accidents which could result in hematoma (which is bleeding under the skin). Also u could have Hemarthrosis, which is (bleeding in the joints). This disorder can cause immobility and can become a defect if not treated. You could also bleed into your muscles, which can cause redness. Hemophilia can be treated according to your age, your health, and your medical history.The probability of your son or daughter having hemophilia depends on a couple of factors. The main factor in this is the sex of your offspring; a male child will have a much greater chance of having hemophilia then a female child will, thus making hemophilia a sex-linked disease. All of the possible combinations of this are attached. The second factor is whether the mother or father have hemophilia or are they a carrier of it. An example of a family with hemophilia is non.
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