Hemophilia is a hereditary disorder impairing blood clotting, leading to frequent bleeding episodes. Early diagnosis and treatment are crucial to managing symptoms and preventing complications. The condition primarily affects males and involves deficiencies in clotting factors VIII or IX. Regular infusions and medical oversight help individuals maintain quality of life and reduce long-term damage.

Hemophilia is a genetic bleeding disorder characterized by the blood's inability to clot effectively. Individuals with hemophilia often experience spontaneous bleeding into joints, muscles, and tissues, which can lead to long-term damage if not properly managed. This condition is inherited, predominantly affecting males due to its X-linked inheritance pattern. Types A and B are caused by shortages of clotting factors VIII and IX, respectively. Treatment typically includes regular infusions of these clotting factors or medications such as DDAVP. Early detection through blood tests and consistent care are essential for preventing serious health issues.