Yang Yang, Zhang Jie
Genetic Diagnosis Center, The Affiliated Hospital of Kunming University of Science and Technology,Kunming 650032, Yunnan Province, China.
Genetic Diagnosis Center, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases,The First People's Hospital of Yunnan Province, Kunming 650032, Yunnan Province, China. E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Feb;25(1):276-280. doi: 10.7534/j.issn.1009-2137.2017.01.050.
Thalassemia is a single-gene disorder resulting from globin chain synthesis impairment because of the mutation or deletion of globin gene, such as α- and β-thalassemia. Thalassemia occurs with high frequencies in tropical and subtropical regions, primarily in Southeast Asian, Middle Eastern, African and Mediterranean populations. It has been reported that thalassemia is prevalent and variable in southern China, including Guangdong, Guangxi, Guizhou, Yunnan and so on. The spectra of globin gene mutations are diverse and characterized by ethnicity and region in southern China. Analysis of the thalassemia gene mutation types is beneficial to develop the measures to prevention and control the thalassemia. The molecular mechemisms and epidemiology of thalassemia as well as spectra of thalassemia gene mutations in southern China are reviewed.
地中海贫血是一种单基因疾病,由于珠蛋白基因的突变或缺失导致珠蛋白链合成受损,如α和β地中海贫血。地中海贫血在热带和亚热带地区高发,主要见于东南亚、中东、非洲和地中海人群。据报道,地中海贫血在中国南方,包括广东、广西、贵州、云南等地普遍存在且具有多样性。中国南方珠蛋白基因突变谱多样,具有种族和地域特征。分析地中海贫血基因突变类型有助于制定预防和控制地中海贫血的措施。本文综述了地中海贫血的分子机制、流行病学以及中国南方地中海贫血基因突变谱。