Haemophilia can be defined as a bleeding disorder that is caused by the deficiency of the clotting factors. The differences between Haemophilia A and B are in the low level – Haemophilia A means low levels of factor (8) and Haemophilia B is low levels of factor (9). Due to the differences in the factors, the same leads to a difference in treatment – Haemophilia A needs to be treated with factor 8 and Haemophilia B with factor 9 replacement. Giving factor 8 to someone with Haemophilia B won’t help to stop the bleeding.
Haemophilia A and B are both bleeding disorders passed on at birth through the genes and are caused by a low level or absence in one of the ‘factors’ normally found in the blood that help make a stable blood clot.
A bad blood clot will mean that a person is at risk of bleeding internally, and most often inside the joints or muscles. The person is also at risk of re-bleeding when the poor blood clot that is formed breaks down too soon.
People with zero levels of a factor are described as having severe haemophilia, and these people are at most risk of bleeding. People with higher levels up to the normal ranges are described as having moderate or mild haemophilia, and the risk of bleeding is less for someone with mild haemophilia.
Hemophilia A and B have different causal mutations; as a result, 35% of patients with haemophilia B have severe disease, compared with 45% of patients with haemophilia A.
Signs & Symptoms of Hemophilia
The signs and symptoms of Hemophilia are excessive/prolonged bleeding. Bleeding can be external or internal. The symptoms depend on the Hemophilia type (A or B) and severity (mild, moderate, or severe).
Other symptoms associated with Hemophilia: