The difference between hemophilia and leukemia

The differences between hemophilia and leukemia are as follows: 1. Hemophilia: It is a genetic, benign disease, but potentially life-threatening. It is a clear bleeding disorder, classified into types A and B. In infants with hemophilia, characteristic or visibly abnormal bleeding may be noticed when the umbilical cord is cut at birth. Even without external injury, patients may experience spontaneous bleeding. Recurrent bleeding can lead to poor absorption and result in joint and muscle dysfunction, such as impaired knee movement. Many adult males may require crutches or wheelchairs. The gene responsible for hemophilia is located on the X chromosome, typically carried by females while affecting males. 2. Leukemia: It is a malignant disease, primarily characterized by symptoms such as fever, bleeding, and fatigue. Without treatment, survival time for leukemia patients is short, especially for those with acute leukemia, who may survive only a few months.