Hemophilia, a hemorrhagic disease, is a genetic defect in the substance that prevents blood from coagulation. Losses expose patients to bleeding under the skin or in the joints or under the muscles when exposed to any injury or minor injury. This substance consists of several proteins working together to help blood clot. This situation requires a long time to clot the blood and sometimes it is not possible to stop bleeding only by giving the needle the missing worker, which works to stop bleeding. Most people are exposed to small vessel ruptures in different tissues of the body, as a result of simple pressure, but in the ideal state of health, blood clotting quickly and not aware of the person. However, a person with hemophilia can bleed longer as a result of such pressure, so many cases of bleeding occur without cause.
There are several types and forms of this disease, which are divided according to the severity of the degree of hemorrhage, the most important type (A), caused by a deficiency in the eighth factor of the clotting, is the most dangerous types of hemophilia, which is 85% of the total cases, where the symptoms of recurrent self-bleeding. Its symptoms are bleeding after bruising or minor strokes.
There are several types and forms of this disease, which are divided according to the severity of the degree of hemorrhage, the most important type (A), caused by a deficiency in the eighth factor of the clotting, is the most dangerous types of hemophilia, which is 85% of the total cases, where the symptoms of recurrent self-bleeding. Its symptoms are bleeding after bruising or minor strokes.