β-地中海贫血(以下简称β-地贫)是世界性顽症之一,它是一种遗传性贫血,其分子基础是由于β-基因缺失或功能缺乏,使β-珠蛋白链不能合成导致早期造血障碍。其治疗以输血为主,有的用5氮胞苷(Azac),阿糖胞苷(Arac)羟基脲(HU)等化疗药物治疗。刘氏曾报告马利兰虽能明显提高贫血恒河猴的r-基因表达,使HbF(抗碱血红蛋白)合成,临床上也有一定的效果,但上述这些药物均有很强的副反应。我们根据中医肾藏精生髓”的理论,采用滋补肾阴生血法,用中国神方丙 Beta-thalassemia (hereinafter referred to as β-thalassemia) is one of the world’s chronic diseases. It is an inherited anemia. Its molecular basis is due to the lack of β-gene deletion or lack of function, so that the β-globin chain cannot be synthesized leading to early Hematopoietic disorders. The treatment is mainly blood transfusion, and some are treated with acetylcytidine (Azac), cytarabine (Arac) hydroxyurea (HU) and other chemotherapy drugs. Liu has reported that Malilan can significantly increase the expression of r-genes in anemia rhesus monkeys and synthesize HbF (alkaline hemoglobin), which has a certain clinical effect, but these drugs have strong side effects. According to the theory of the essence of Chinese medicine in kidneys, we use nourishing kidney yin and blood and use Chinese God C