Thalassemia: Detection, Management, Prevention & Curative Treatment
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Published:
Feb 18, 2011
Keywords:
Thalassemia syndrome Genetic disease Hemolytic anemia
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Abstract
Thalassemia syndromes are inherited genetic diseases caused by mutation of alpha or beta globin genes, which result in abnormal hemoglobin synthesis.
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How to Cite
1.
Vanichsetakul P. Thalassemia: Detection, Management, Prevention & Curative Treatment. BKK Med J [Internet]. 2011 Feb. 18 [cited 2024 Dec. 27];1(1):113. Available from: https://he02.tci-thaijo.org/index.php/bkkmedj/article/view/217685
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Continue Medical Education (CME)
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References
1. Vichinsky E, Levine L, Bhatia S, et al. Standards of Care Guidelines for Thalassemia. Children’s Hospital & Research Center Oakland, U.S.A. 2008.
2. Cappellini M-D, Cohen A, Eleftheriou A, Piga A, Porter J, Taher A. Guidelines for the Clinical Management of Thalassaemia 2nd Revised Edition November 2008. Thalassaemia International Federa-tion, Cyprus.
3. Dumars K W, Boehem C, Eckman JR, et al. Practical guide to the diagnosis of thalassemia. Am J Med Genet 1996;62:29-37
2. Cappellini M-D, Cohen A, Eleftheriou A, Piga A, Porter J, Taher A. Guidelines for the Clinical Management of Thalassaemia 2nd Revised Edition November 2008. Thalassaemia International Federa-tion, Cyprus.
3. Dumars K W, Boehem C, Eckman JR, et al. Practical guide to the diagnosis of thalassemia. Am J Med Genet 1996;62:29-37