Hemophilia Term paper

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Hemophilia

Tim Poisal Biology-2nd period

Hemophilia is a genetic blood disease, which is characterized by the

inability of blood to clot, or coagulate even from minor injuries. This disease

is caused by an insufficiency of certain blood proteins, called factors, that

participate in blood clotting and often by sudden gene mutation. Therefore,

with the absence of factors, the blood clotting process is prolonged. There are

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. In

the second most common form of hemophilia, hemophilia B (also known as Christmas

disease), factor IX is absent.

The condition appears when the person is born. Also, the disease is

hereditary, passed on from parent to child. Because of it's genetic makeup,

hemophilia is carried by females however those affected are almost always males.

In one-third of all cases hemophilia thought to be caused by spontaneous gene

mutation with no family history. This is how females are able to be...

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