珠蛋白生成障碍性贫血(国外英文资料).docVIP

珠蛋白生成障碍性贫血(国外英文资料) The standard of diagnosis and efficacy of haematological diseases in the formation of aplastic anemia A central tip: thalassemia is also known as thalassemia, or thalassemia, or thalassemia, or thalassemia. In November 1987, at a national hemolytic anemia in Shanghai special conferences and in October 1988 in luoyang national pediatric haematology meeting to discuss, and developed the disease diagnostic criteria for each model. Based on the above criteria, the diagnostic criteria for the proposed diagnosis are as follows Diagnostic criteria Domestic diagnostic criteria ????? Thalassemia is also known as thalassemia, or thalassemia, or thalassemia, or thalassemia, or thalassemia. In November 1987, at a national hemolytic anemia in Shanghai special conferences and in October 1988 in luoyang national pediatric haematology meeting to discuss, and developed the disease diagnostic criteria for each model. Based on the above criteria, the diagnostic criteria for the proposed diagnosis are as follows. One, beta-globin formation of disordered anemia 1, the heavy (1) clinical manifestations: anemia, jaundice, liver splenomegaly. Children patients with dysplasia, mental retardation, bone changes from broadening zygomatic uplift, eye, nose, X-ray visible plating trabecular bone stripes clear straight hair sample and so on. (2) laboratory examination: HB is less than 60g/L, with low blood cell hypohaematocytic anemia; Erythrocytes are heterogeneous and heterogeneous, and have target red blood cells (10% or more). There is an increase in the network. The red blood cell system in the bone marrow is hyperplasia. Hemoglobin electrophoresis: HBF is greater than 30%. (3) the family study could prove that the parents of the patient were all light-weight beta-globin formation of aplastic anemia. Conform to the clinical manifestations, have severe hemolytic anemia, HBF is more than 30%, and with the exception of HBF, increases the generation of other globin barrier an