Department of Pathology and Clinical Biochemistry, Queen Mary Hospital , Hong Kong SAR , China and.
Crit Rev Clin Lab Sci. 2013 Nov;50(6):125-41. doi: 10.3109/10408363.2013.847236.
Thalassemia is the most common monogenic inherited disease worldwide and it affects most countries to various extents. This review summarizes the current approaches to phenotypic and genotypic diagnosis of thalassemia in clinical practice. Prevention strategies that encompass carrier screening, genetic counseling and prenatal diagnosis are discussed. The importance of public education and an awareness of a changing perception regarding this group of diseases are emphasized. It also addresses the impact of the rapidly increasing knowledge in disease severity modification by hemoglobin F (Hb F).
地中海贫血是全球最常见的单基因遗传性疾病,在不同程度上影响着大多数国家。本文综述了目前在临床实践中用于地中海贫血表型和基因型诊断的方法。讨论了涵盖携带者筛查、遗传咨询和产前诊断的预防策略。强调了公众教育的重要性以及对这组疾病的认识正在发生变化。它还涉及到由血红蛋白 F(Hb F)引起的疾病严重程度改变的快速增加的知识的影响。