| Literature DB >> 20113289 |
Cui-Mei Zhang1, Ying Wang, Li-Shao Gao, Jian-Hui Gao, Xiao-Ling He, Hua-Jun Feng, Jia-Luo Liao.
Abstract
Beta-THAlassemia (beta-thal) is one of the most common genetic diseases in southern China. In order to obtain detailed epidemiology data to be used for primary prevention programs, we have analyzed 2,055 independent subjects living in Zhongshan City, Guangdong Province, People's Republic of China (P.R. China), by using hematological biochemical screening and DNA technology. The results indicate a higher prevalence (3.07%) of beta-thal and coinheritance of alpha- and beta-thal (0.49%) than previously reported for Guandong Province. Ten beta-thal mutations were found in 63 independent chromosomes. The four most common mutations [codons 41/42 (-TCTT), IVS-II-654 (C>T), -28 (A>G), codon 17 (A>T)] accounted for 90.46% of the total. The uncommon mutations profile was different from that of other cities in Guangdong Province and the rare mutation IVS-II-2 (-T), once reported in Hong Kong, was also detected. This study will contribute to the development of prevention strategies in the region, allowing better genetic counseling and prenatal diagnosis of beta-thal.Entities:
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Year: 2010 PMID: 20113289 DOI: 10.3109/03630260903547724
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849