β-地中海贫血(Beta-thalassemia)的颅骨表现 这是一种遗传性血液疾病,属于地中海贫血(Thalassemia)的一种类型。它是由于编码血红蛋白β链的基因(HBB基因)发生突变,导致β-珠蛋白(血红蛋白的重要组成部分)...
Beta-thalassemia is caused by the reduced (beta) or absent (beta) synthesis of the beta globin chains of the hemoglobin tetramer. Three clinical and hematological conditions of increasing severity are recognized, i.e., the beta-thalassemia carrier state, thalassemia intermedia, and thalassemia major...
beta-thalassemia [英]'bi:təθəlɑ:s'i:mɪə [美]'bi:təθəlɑ:s'i:mɪr [医]β-地中海贫血 [例句]Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children. β-地中海贫血;造血干细胞移植;单倍体;儿童. 手机提问的朋友在客户端右上角...
The meaning of BETA-THALASSEMIA is thalassemia in which the longer hemoglobin chain is affected and which comprises Cooley's anemia in the homozygous condition and thalassemia minor in the heterozygous condition.
beta-thalassemia [英]'bi:təθəlɑ:s'i:mɪə[美]'bi:təθəlɑ:s'i:mɪr [医]β-地中海贫血 [例句]Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children.β-地中海贫血；造血干细胞移植；单倍体；儿童。
The gene for beta thalassemia is not evenly distributed among different groups of people. It is, for example, relatively more frequent in people of Italian and Greek origin, both of whom are people from the Mediterranean. Because of this, thalassemia major has been called Mediterranean anemia. ...
thalassemia vs. anemia Discover More Example Sentences Beta thalassemia mainly affects people of Mediterranean, south Asian, south-east Asian and Middle Eastern backgrounds. FromBBC Another genetic analysis found that women with an inherited blood disorder called beta thalassemia, which produces chronically...
In beta thalassemia, the degree of globin chain imbalance is determined by the nature of the mutation of the β-gene. β° refers to the complete absence of production of β-globin on the affected allele. βrefers to alleles with some residual production of β-globin. The homozygous state ...
The meaning of ALPHA-THALASSEMIA is thalassemia in which the hemoglobin chains designated alpha are affected.
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual