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Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia

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dc.contributor.author Premawardhena, A.P. en_US
dc.contributor.author Fisher, C.A. en_US
dc.contributor.author Fathihu, F. en_US
dc.contributor.author de Silva, S. en_US
dc.contributor.author Perera, W. en_US
dc.contributor.author Peto, T.E. en_US
dc.contributor.author Olivieri, N.F. en_US
dc.contributor.author Weatherall, D.J. en_US
dc.date.accessioned 2014-10-29T09:19:17Z
dc.date.available 2014-10-29T09:19:17Z
dc.date.issued 2001 en_US
dc.identifier.citation Lancet.2001; 357(9272): 1945-46 en_US
dc.identifier.issn Lancet Publishing Group en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/1484
dc.description.abstract Chronic hyperbilirubinaemia, gallstone formation, and gall bladder disease are unusually common in people with haemoglobin E beta thalassaemia in Sri Lanka. To determine whether this has a genetic basis we compared the bilirubin levels and frequency of gallstones in patients with different alleles of the UGT*1 gene. There was a significantly higher bilirubin level in those with the 7/7 genotypes compared with 6/6 and 6/7 genotype (p=0.032 and 0.0015 respectively), who also appeared more prone to gallstone formation. These results suggest that the UGT*1 genotpe is of importance in the genesis of gallstones in this population of patients.
dc.title Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia en_US
dc.type Article en_US
dc.identifier.department Medicine en_US


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