Iron Status In Beta Thalassaemia Trait In Adult

  • Md Maruf-Ur-Rahman Lecturer, Department of Biochemistry, Dhaka National Medical College
  • Kalyan Kirtania Assistant Professor, Department of Biochemistry, Johurul Islam Medical College
  • Md Mahbubur Rahman Assistant Professor, Department of Biochemistry, Pabna Medical College
  • Nasima Sultana Associate Professor and Head, Department of Biochemistry, Dhaka Medical College
  • Md Shamsur Rahman Professor and Head, Department of Biochemistry, Dhaka National Medical College
  • Selina Ahmed Professor and Head, Department of Biochemistry, Popular Medical College
Keywords: Iron status, Beta Thalassaemia trait

Abstract

Microcytic hypochromic anaemia is one of the commonest blood picture in Bangladeshi population. A vast majority of such cases have iron deficiency. In Bangladesh about 3% of total population that is about 3.6 million people with a microcytic hypochromic blood picture are beta thalassaemia trait. However iron deficiency may be associated with beta thalassaemia trait. Such patients are treated with iron to improve their anaemia. But the subjects of beta thalassaemia trait often have normal iron level. So, by observing microcytic hypochromic blood picture, supplementation of iron to that cases produce iron overload and may produce organ dysfunction. The study of serum ferritin was carried out on 50 confirmed cases of beta thalassaemia trait and 50 cases of healthy individuals. Estimation of serum ferritin level was done by Dimension RxL Max (Automatic Biochemistry Analyzer). The results show that serum iron level was normal in beta thalassaemia trait as like as healthy individuals.

DOI: http://dx.doi.org/10.3329/jdnmch.v17i2.12211

J. Dhaka National Med. Coll. Hos. 2011; 17 (02): 21-24

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Abstract
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Published
2012-10-17
How to Cite
Maruf-Ur-Rahman, M., Kirtania, K., Rahman, M., Sultana, N., Rahman, M., & Ahmed, S. (2012). Iron Status In Beta Thalassaemia Trait In Adult. Journal of Dhaka National Medical College & Hospital, 17(2), 21-24. https://doi.org/10.3329/jdnmch.v17i2.12211
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Original Articles