Common Types of Hemophilia
Hemophilia is a rare blood disorder that occurs when the blood doesn’t clot normally because the patient lacks sufficient blood-clotting proteins (or clotting factors). Patients with hemophilia often bleed for a longer duration after surgery, trauma, or injury, and may even risk non visual internal bleeding (i.e., head, elbows, ankles, and knees) when blood doesn’t clot sufficiently. According to the U.S. Center for Disease Control and Prevention (CDC), one in every 5000 born will be hemophiliacs. Approximately 20,000 residents in America suffer from hemophilia. When a person bleeds, what normally happens is that the blood pulls blood cells together to create a clot that prevents bleeding. Some blood particles encourage clotting to take place. Hemophilia takes place when you have complications on these clotting factors. Signs and symptoms of hemophilia may include: Excessive bleeding from injuries or cuts, or after dental work or surgery Deep and large bruises Swelling, pain, and tightness in the joints Blood in stool or urine The main types of hemophilia include: 1. Hemophilia type A Hemophilia is caused by a defective or missing factor VIII protein. It is thought to be genetically transferred from parent to child as the X chromosome carries the hemophilia gene, which is inherited in an X-intertwined formula.