Literature DB >> 16540409

The prevalence and spectrum of thalassemia in Shenzhen, Guangdong Province, People's Republic of China.

Zesong Li1, Fangfang Li, Ming Li, Runjun Guo, Wen Zhang.   

Abstract

Thalassemia (thal) is the most common autosomal disorder in southern China. The aim of the present study was to investigate the prevalence and spectrum of thalassemia mutations in the population of Shenzhen, Guangdong Province. In total, 3,711 samples from two hospitals in Shenzhen were subjected to hematological and molecular analysis. Of these, 241 (6.49%) were carriers of thalassemias, of which 161 (4.34%) had alpha-thal, 74 (1.99%) had beta-thal, and six (0.16%) had both alpha- and beta-thal. Three deletional and one nondeletional alpha-thal mutation, and nine beta-thal mutations were identified. Compared with other areas in Guangdong Province, the prevalence of thalassemia in Shenzhen was lower, while there was no evident difference for the spectrum of mutations. These results will provide a reference for prenatal testing and genetic counseling in the area.

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Year:  2006        PMID: 16540409     DOI: 10.1080/03630260500453818

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  7 in total

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2.  Cut-Off Values of Hematologic Parameters to Predict the Number of Alpha Genes Deleted in Subjects with Deletional Alpha Thalassemia.

Authors:  Diego Velasco-Rodríguez; Carlos Blas; Juan-Manuel Alonso-Domínguez; Gala Vega; Carlos Soto; Aránzazu García-Raso; Pilar Llamas-Sillero
Journal:  Int J Mol Sci       Date:  2017-12-13       Impact factor: 5.923

3.  Molecular analysis of alpha- and beta-thalassemia in Meizhou region and comparison of gene mutation spectrum with different regions of southern China.

Authors:  Heming Wu; Qingyan Huang; Zhikang Yu; Zhixiong Zhong
Journal:  J Clin Lab Anal       Date:  2021-11-09       Impact factor: 2.352

4.  The prevalence and outcomes of α- and β-thalassemia among pregnant women in Hubei Province, Central China: An observational study.

Authors:  Yao Cheng; Miaomiao Chen; Jiazhi Ye; Qin Yang; Ronggui Wang; Shulian Liu; Rui Su; Jieping Song; Tangxinzi Gao; Runhong Xu; Feixia Zhao; Peili Zhang; Guoqiang Sun
Journal:  Medicine (Baltimore)       Date:  2022-03-04       Impact factor: 1.817

5.  Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China.

Authors:  Min Lin; Ying-Fang Wen; Jiao-Ren Wu; Qian Wang; Lei Zheng; Gui-Rong Liu; Yue Huang; Hui Yang; Fen Lin; Xiao-Fen Zhan; Chun-Ping Lin; Hui-Tian Yang; Qiu-Qing Weng; Fen-Ting Huang; Yuan Wang; Mei-Qiong Yao; Hui-Zhou Chen; Di-Hong Wu; Jing-Bo Zeng; Ri-Xin Zeng; Hua Yang; Gui-Cai Li; Min Lu; Juan-Juan Zhu; Long-Xu Xie; Jun-Li Wang; Li-Ye Yang
Journal:  PLoS One       Date:  2013-02-01       Impact factor: 3.240

6.  The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China.

Authors:  Aihua Yin; Bing Li; Mingyong Luo; Longchang Xu; Li Wu; Liang Zhang; Yuanzhu Ma; Tingting Chen; Shuang Gao; Juqing Liang; Hao Guo; Danqing Qin; Jicheng Wang; Tenglong Yuan; Yixia Wang; Wei-wei Huang; Wen-Fei He; Yanxia Zhang; Chang Liu; Sujian Xia; Qingshan Chen; Qingguo Zhao; Xiaozhuang Zhang
Journal:  PLoS One       Date:  2014-02-27       Impact factor: 3.240

7.  Analysis of genotype distribution of thalassemia and G6PD deficiency among Hakka population in Meizhou city of Guangdong Province.

Authors:  Heming Wu; Qiuyan Zhu; Hua Zhong; Zhikang Yu; Qunji Zhang; Qingyan Huang
Journal:  J Clin Lab Anal       Date:  2019-12-03       Impact factor: 2.352

  7 in total

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