Literature DB >> 19814675

Thalassemia incidence and treatment in China with special reference to Shenzhen City and Guangdong province.

Chang-Gang Li1, Chun-Fu Li, Qi Li, Ming Li.   

Abstract

According to the data from different screening studies, thalassemia is the most commonly seen hereditary hemolytic disease in China. The reported prevalence of thalassemia carriers varies but it is most prevalent in Southern China. In the past, the outcome of patients with thalassemia major has been very poor due to unfavorable economic background. With economic improvement in the past 10 years, increasing number of patients can get regular transfusion and chelation, and more patients can be treated by hemopoietic stem cell transplantation. A better prevention network has been built up over the years, but there are still babies being born with severe forms of thalassemia every year. A more comprehensive preventive program and public education are vital.

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Year:  2009        PMID: 19814675     DOI: 10.3109/03630260903211698

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


  7 in total

1.  Optimization and application of a dried blood spot-based genetic screening method for thalassemia in Shenzhen newborns.

Authors:  Wei Wen; Meng Guo; Hong-Bing Peng; Li Ma
Journal:  World J Pediatr       Date:  2019-04-27       Impact factor: 2.764

2.  Karyomapping in preimplantation genetic testing for β-thalassemia combined with HLA matching: a systematic summary.

Authors:  Jing Wang; Bao-Min Lu; Rong Li; Jing Guo; Yan Xu; Jia-Fu Pan; Yan-Hong Zeng; Can-Quan Zhou; Yan-Wen Xu
Journal:  J Assist Reprod Genet       Date:  2019-11-22       Impact factor: 3.412

3.  Cat-D: a targeted sequencing method for the simultaneous detection of small DNA mutations and large DNA deletions with flexible boundaries.

Authors:  Ru Hong; Udita Chandola; Li-Feng Zhang
Journal:  Sci Rep       Date:  2017-11-16       Impact factor: 4.379

4.  Prioritizing congenital syphilis control in south China: a decision analytic model to inform policy implementation.

Authors:  Nicholas X Tan; Chara Rydzak; Li-Gang Yang; Peter Vickerman; Bin Yang; Rosanna W Peeling; Sarah Hawkes; Xiang-Sheng Chen; Joseph D Tucker
Journal:  PLoS Med       Date:  2013-01-22       Impact factor: 11.069

5.  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

6.  Predicting future blood demand from thalassemia major patients in Hong Kong.

Authors:  Eric H Y Lau; Xiu-Qing He; Cheuk-Kwong Lee; Joseph T Wu
Journal:  PLoS One       Date:  2013-12-11       Impact factor: 3.240

7.  Investigating the Reliability of HbA1c Monitoring for Blood Glucose Control During Late Pregnancy in Patients with Gestational Diabetes Mellitus (GDM) with and without β-Thalassemia Minor.

Authors:  Xueqin Zhang; Yunshan Xiao; Yanfeng Fan
Journal:  Diabetes Ther       Date:  2018-10-04       Impact factor: 2.945

  7 in total

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