Meyer L M, Adams J G, Steinberg M H, Miller I E, Stokes N
Am J Hematol. 1987 Apr;24(4):429-32. doi: 10.1002/ajh.2830240413.
Results of the Veterans Administration Sickle Cell Program for a period of 10 years are presented. We screened 370,250 patients; 404,341 attended educational sessions, and 38,347 had individual counseling sessions. Sickle cell trait was present in 6.4% of patients, and HbC trait was present in 1.8%. The clinically significant disorders HbSC disease, sickle cell anemia, and sickle beta thalassemia were present in 0.41% of individuals screened. A large number of uncommon variants were detected. The program enhanced the awareness of and the approach to evaluation of hemoglobinopathies.
本文展示了退伍军人管理局镰状细胞项目10年的成果。我们筛查了370250名患者;404341人参加了教育课程,38347人接受了个人咨询。6.4%的患者存在镰状细胞特征,1.8%的患者存在HbC特征。在筛查的个体中,具有临床意义的疾病HbSC病、镰状细胞贫血和镰状β地中海贫血占0.41%。检测到大量罕见变异。该项目提高了对血红蛋白病的认识以及评估方法。