Can hemophilia be cured?
hemophilia has no complete cure at present. Therefore, we should pay attention to comprehensive treatment. In addition to the corresponding infusion of various coagulation factor products during bleeding, traditional Chinese medicine plays a positive role in the rehabilitation after bleeding and the treatment and prevention of hemophilia arthritis.
hemophilia is a lifelong bleeding disease. The carrier should be given antenatal care to control the birth of the child and carrier, so as to reduce the incidence rate of the population and achieve eugenics.
how long can hemophilia live
although there is no cure for hemophilia, hemophilia patients can live a healthy life after treatment. Hemophilia is not a fatal disease. As long as patients supplement coagulation factors in time and take good care of their daily life, they are no different from normal people in appearance. Hemophilia patients can work, live and participate in social activities like normal people without affecting people’s natural life span.
without treatment, people with severe hemophilia will be difficult to go to school or work normally. They may be disabled, difficult to walk or do some simple activities, and even die early.
hemophilia examination
screening test: platelet count, bleeding time and clot withdrawal time were normal, coagulation time, partial thromboplastin time and thromboplastin production time were prolonged, and serum prothrombin time was shortened.
qualitative test: thromboplastin production test and correction test. Simple thromboplastin production correction test has diagnostic significance for hemophilia typing: Hemophilia A a can be corrected by normal barium sulfate adsorbed plasma but not by normal serum. Hemophilia B can not be corrected by normal barium sulfate adsorbed plasma, but can be corrected by normal serum. Hemophilia C can be corrected by normal barium sulfate adsorbed plasma and normal serum.
clinically, there are many blood diseases and hemophilia with similar symptoms, which should be distinguished. For example, it should be distinguished from vascular pseudohemophilia. Vascular pseudohemophilia is caused by the absence or decrease of Ⅷ R, Ag and Ⅷ R: WF, and the decrease of Ⅷ: C activity may also be caused. Typical vascular pseudohemophilia has a family history, autosomal dominant inheritance, that is, both men and women can get sick, and both parents can inherit it. The main clinical manifestations are mucosal and subcutaneous bleeding, and a few joint and muscle bleeding, but generally there is no joint deformity, the bleeding time is prolonged or the aspirin tolerance test is positive, and the Ⅷ: C, Ⅷ R: RCOF and Ⅷ R: AG are reduced, which can be helpful for diagnosis and differential diagnosis.
hemophilia is mostly caused by heredity. Variant vascular pseudohemophilia can be autosomal recessive inheritance. Parents can have no clinical manifestation, no genetic history, serious bleeding symptoms and bleeding time. One or several items of Ⅷ R: RCOF are normal, but Ⅷ R: Ag cross immunoelectrophoresis is abnormal, which can help to identify.
hemophilia is more common in type A, and bleeding symptoms are the main manifestation of the disease. For this patient, there is no better medical treatment, and blood transfusion can only be the main treatment.