Journal of Tropical Pediatrics Advance Access published online on June 20, 2005
Journal of Tropical Pediatrics, doi:10.1093/tropej/fmi052
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1 Department of Paediatrics, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
* To whom correspondence should be addressed.
Original Papers
Characterisation of
-globin Gene Mutations in Malaysian Children: A Strategy for the Control of -Thalassaemia in a Developing Country
2 Department of Molecular Medicine, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
3 Department of Pathology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
Meow-Keong Thong, E-mail: thongmk{at}um.edu.my
Abstract 
-thalassaemia major, an autosomal recessive hemoglobinopathy, is one of the most common single gene disorders in multi-racial Malaysia. The control of -thalassaemia major requires a multi-disciplinary approach that includes population screening, genetic counselling, prenatal diagnosis and the option of termination of affected pregnancies. To achieve this objective, the molecular characterisation of the spectrum of -globin gene mutations in each of the affected ethnic groups is required. We studied 88 consecutive unrelated individuals and their respective families with -thalassaemia (74 -thalassaemia major, 12 HbE--thalassaemia, 2 with HbE homozygotes) and four individuals with -thalassaemia trait that contributed a total 180 alleles for study. Using a 2-step molecular diagnostic strategy consisting of amplification refractory mutation system (ARMS) to identify the 8 most common mutations followed by other DNA-based diagnostic techniques, a total of 177 (98.3 per cent) of the 180 -thalassaemia alleles were characterised. One out of 91 (1 per cent) of the Chinese alleles, one out of 46 (2.2 per cent) Malay alleles and one out of two Indian alleles remained unknown. A 100 per cent success rate was achieved in studying the Kadazandusun community in this study. A strategy to identify -globin gene mutations in Malaysians with -thalassaemia is proposed based on this outcome.
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