International Journal of Hematology

, Volume 76, Supplement 2, pp 96–104

β-Thalassaemia prototype of a single gene disorder with multiple phenotypes

  • Swee Lay Thein
Thalassemia and Hemoglobinopathy

DOI: 10.1007/BF03165097

Cite this article as:
Thein, S.L. Int J Hematol (2002) 76(Suppl 2): 96. doi:10.1007/BF03165097


As the defective genes for more and more genetic disorders become unravelled, it is clear that patients with the same genotype can have many different clinical conditions even in monogenic disorders. The remarkable phenotypic diversity of the βthalassaemias is prototypical of how the wide spectrum in disease severity can be generated. The most reliable and predictive factor of disease phenotype is the nature of the mutation at the β-globin locus itself. However, relating phenotype to genotype is complicated by the complex interaction of the environment and other genetic factors at the secondary and tertiary levels, some implicated, and others, as yet unidentified. This article reviews the clinical and haematological diversity encountered in βthalassaemia and their relationship with the under-lying genotypes.

Copyright information

© The Japanese Society of Hematology 2002

Authors and Affiliations

  • Swee Lay Thein
    • 1
  1. 1.Department of Haematological Medicine, Guy’s, King’s & St Thomas’ School of MedicineDenmark Hill CampusLondonUK

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