Hemophilia B

Hemophilia B is a genetic disorder that affects blood clotting. It occurs when the body lacks enough of a specific protein called factor IX, which is crucial for forming blood clots. This deficiency leads to prolonged bleeding, especially after injury or surgery, and can cause spontaneous bleeding into joints and muscles. Hemophilia B is inherited, mainly affecting males, while females can be carriers. Treatments include infusions of factor IX to help control bleeding episodes and prevent complications. With proper management, individuals with Hemophilia B can lead healthy lives.