Treatment for different types of hemophilia
Hemophilia A and B are hereditary conditions and affect young children and men more than women. Screening at birth and frequent screening can ensure that one is aware of the risks and can protect their families accordingly. There is no cure yet for the condition and treatment focuses on controlling the bleeding and improving associated symptoms that are caused by hemophilia. A family tree, DNA test or a blood test will confirm if one is a hemophilia carrier. For those who are known carriers of hemophilia, tests for their newborn will be done at birth wherein blood may be drawn from the newborn or its umbilical cord. After this, coagulation tests done in certified laboratories are recommended. Based on the test results, doctors will work out a treatment protocol or advise a set of precautions that has to be followed to safeguard the child from preventable injuries and trauma. As there is no permanent cure yet for any type of hemophilia, the doctors begin treatment intending to improve or increase the clotting factors, stop the continuous bleeding, and reduce pain, dizziness, or seizures. The treatment also attempts to stop and prevent other complications that arise from bleeding. It is also crucial that any internal bleeding is diagnosed early and treated accordingly.