Hajjar F M, Pearson H A
Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut.
J Pediatr. 1994 Sep;125(3):490-2. doi: 10.1016/s0022-3476(05)83304-9.
Three adult patients with beta-thalassemia intermedia were treated with hydroxyurea. Each had a significant but transient rise in total hemoglobin level associated with a variable increase in hemoglobin F.
三名中间型β地中海贫血成年患者接受了羟基脲治疗。每名患者的总血红蛋白水平均有显著但短暂的升高,同时血红蛋白F也有不同程度的增加。