Ghani Rubina, Manji Mehdi A, Ahmed Nikhat
Department of Biochemistry, University of Karachi, Karachi, Pakistan.
Southeast Asian J Trop Med Public Health. 2002 Dec;33(4):855-61.
A brief survey of abnormal hemoglobin variants among the major ethnic groups of Karachi was conducted; 202,600 subjects were studied. Patients with low hemoglobin (Hb), low mean cell volume (MCV) and mean cell hemoglobin (MCH) including anemia, microcytosis, hypochromic hemolysis and target cells, were refered for the identification of hemoglobinopathy by molecular methods. Population screening showed that 60% had iron-deficiency anemia and 40% had hemolytic anemia, of which 20.6% was due to beta-thalassemia major, 13% beta-thalassemia trait, 5.1% sickle cell disease, 0.76% hemoglobin D Punjab (HbD Punjab), 0.32% hemoglobin C (HbC), and 0.22% hereditary persistence of fetal hemoglobin (HPFH).
对卡拉奇主要族群中的异常血红蛋白变体进行了一项简要调查;共研究了202,600名受试者。血红蛋白(Hb)低、平均红细胞体积(MCV)和平均红细胞血红蛋白(MCH)低的患者,包括贫血、小红细胞症、低色素性溶血和靶形细胞,通过分子方法进行血红蛋白病鉴定。人群筛查显示,60%患有缺铁性贫血,40%患有溶血性贫血,其中20.6%是由于重型β地中海贫血,13%是β地中海贫血特征,5.1%是镰状细胞病,0.76%是血红蛋白D旁遮普型(HbD旁遮普型),0.32%是血红蛋白C(HbC),0.22%是胎儿血红蛋白遗传性持续存在(HPFH)。