Department of Pathology, College of Medicine, University of Dohuk, Dohuk City, Iraq.
East Mediterr Health J. 2010 Apr;16(4):381-5.
beta-thalassaemia major and sickle-cell disease are important health problems in Iraq. To provide information for a prevention programme, the frequency of haemoglobin disorders was mapped in Dohuk governorate. A total of 591 couples (1182 individuals) attending health centres for premarital health screening were tested; 44 (3.7%) were found to be carriers of ,-thalassaemia, 14 (1.2%) of the sickle-cell gene and 1 (0.1%) of deltabeta3-thalassaemia. A total of 3 couples (i.e. 5/1000) were at risk of having a child with beta-thalassaemia major, and the estimated number of affected children with a major haemoglobinopathy was 39 per year. The findings stress the importance of a regional prevention programme for haemoglobinopathies based on premarital screening, counselling and prenatal diagnosis.
β-地中海贫血和镰状细胞病是伊拉克的重要健康问题。为了提供预防计划的信息,在杜胡克省对血红蛋白疾病的频率进行了绘图。共有 591 对(1182 人)参加婚前健康检查的医疗中心进行了测试;发现 44 人(3.7%)是β-地中海贫血携带者,14 人(1.2%)是镰状细胞基因携带者,1 人(0.1%)是三角洲β3-地中海贫血携带者。共有 3 对夫妇(即每 1000 对中有 5 对)有生育β-地中海贫血重型患儿的风险,每年估计有 39 名重型血红蛋白病患儿受到影响。这些发现强调了基于婚前检查、咨询和产前诊断的血红蛋白病区域性预防计划的重要性。