Al-Zir Kusai Nasser
Thalassaemia Patient's Friends Association and Hereditary Blood Disease, Damascus, Syria.
Hemoglobin. 2009;33 Suppl 1:S25-7. doi: 10.3109/03630260903346460.
Hemoglobin disorders are highly prevalent in Syria resulting in a significant strain to national resources. To ensure survival and good quality of life of existing patients who are currently almost 8,000 and increasing by almost 800 each year, it is necessary to introduce a national prevention program. This brief report explains the measures that are under discussion currently and proposed for inclusion in a comprehensive control program.
血红蛋白疾病在叙利亚极为普遍，给国家资源带来了巨大压力。为确保目前近8000名且每年增加近800名的现有患者能够存活并拥有良好的生活质量，有必要推行一项全国性预防计划。本简要报告解释了目前正在讨论并提议纳入全面控制计划的各项措施。
