What characterizes hemophilia?

Hemophilia is characterized by a hereditary deficiency in clotting factors, which are essential proteins needed for blood coagulation. Individuals with hemophilia often experience prolonged bleeding after injury or surgery, and may even have spontaneous bleeding episodes without any obvious cause. This condition arises due to genetic mutations that affect the production of clotting factors, particularly factor VIII or factor IX, depending on the type of hemophilia (A or B, respectively).

Understanding the role of clotting factors is crucial for recognizing the implications of hemophilia on a person's health and activity level. Effective management and treatment involve enhancing the individual's ability to produce or receive the deficient factors, allowing for better control of bleeding episodes. The other choices do not relate specifically to hemophilia, as they address different medical conditions involving oxygen transport, white blood cell counts, and dietary iron levels rather than the essential clotting process.