论文部分内容阅读
血红蛋白病(简称Hb病)是一种遗传性疾病,由于血红蛋白分子结构的异常或肽链合成速率的变化而引起。据世界卫生组织(WHO)估计全世界约有一亿多人携带Hb病的基因。近年来国内对17个省(区)市、20个民族十几万人进行了普查,发现了不少异常血红蛋白。广东省是高发区。1980～1981年我们对
Hemoglobinopathy (referred to as Hb disease) is a genetic disease, due to abnormal molecular structure of hemoglobin or peptide chain synthesis rate caused. According to the World Health Organization (WHO), more than 100 million people worldwide carry Hb disease genes. In recent years, the survey of more than 100,000 people in 17 provinces (districts) and 20 ethnic groups in China has revealed many abnormal hemoglobin. Guangdong Province is a high incidence area. 1980 ~ 1981, we are right