Literature DB >> 6165216

Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.

S C Wong, M A Ali, S E Boyadjian.   

Abstract

A trimodal distribution of the amounts of Hb S in 56 sickle cell heterozygotes was observed. The variable amounts of Hb S were directly related to the mean cell volume and the mean cell Hb and were a result of the difference in net synthesis of Hb S due to the presence of the alpha-thalassaemia. Double heterozygotes for the Hb S and alpha-thalassaemia-1 genes, besides having a lower amount of Hb S in the red blood cells, were found to have lower Hb and slightly elevated Hb A2 levels.

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Year:  1981        PMID: 6165216     DOI: 10.1159/000207172

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  2 in total

1.  Can Trimodal Distribution of HbS Levels in Sickle Cell Traits Be Used To Predict the Associated Alpha-Thalassemia For Screening Cases in Central India?

Authors:  B M Warpe; A V Shrikhande; S V Poflee
Journal:  Iran J Pathol       Date:  2016

2.  Some observations on the measurement of haemoglobin A2 and S percentages by high performance liquid chromatography in the presence and absence of alpha thalassaemia.

Authors:  C E Head; M Conroy; M Jarvis; L Phelan; B J Bain
Journal:  J Clin Pathol       Date:  2004-03       Impact factor: 3.411

  2 in total

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