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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 4
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Short Communication

Prevalence of α+-Thalassemia in the Scheduled Tribe and Scheduled Caste Populations of Damoh District in Madhya Pradesh, Central India

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Pages 285-288 | Received 21 Nov 2015, Accepted 27 Feb 2016, Published online: 18 May 2016

References

  • Sengchanh S, Sanguansermsri T, Horst D, et al. High frequency of α thalassemia in the So ethnic group of South Laos. Acta Haematol. 2005;114(3):164–166
  • Weatherall DJ. Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias. Nat Rev Genet. 2001;2(4):245–255
  • Higgs DR, Weatherall DJ. The α thalassaemias. Cell Mol Life Sci. 2009;66(7):1154–1162
  • Harteveld CL, Higgs DR. α-thalassaemia. Orphanet J Rare Dis. 2010;5:13. doi: 10.1186/1750-1172-5-13
  • Allen SJO, Donnell A, Alexander NDE, et al. α+-Thalassemia protects children against disease caused by other infections as well as malaria. Proc Natl Acad Sci U.S.A. 1997;94(26):14736–14741
  • Mockenhaupt FP, Ehrhardt S, Gellert S, et al. α+-Thalassemia protects African children from severe malaria. Blood. 2004;104(7):2003–2006
  • Williams TN, Wambua S, Uyoga S, et al. Both heterozygous and homozygous α+-thalassemias protect against severe and fatal Plasmodium falciparum malaria on the coast of Kenya. Blood. 2005;106(1):368–371
  • Nadkarni A, Phanasgaonkar S, Colah R, et al. Prevalence and molecular characterization of α-thalassemia syndromes among Indians. Genet Test. 2008;12(2):177–180
  • Sen R, Chakrabarti S, Sengupta B, et al. α-Thalassemia among tribal populations of Eastern India. Hemoglobin. 2005;29(4):277–280
  • Chanarin I. Laboratory Haematology: An Account of Laboratory Techniques, 1st ed. London, UK: Churchill Livingstone, 1989
  • Dacie JV, Lewis SM. Practical Haematology, 7th ed. London, UK: Churchill Livingstone, 1991
  • Betke K, Marti HR, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature. 1959;184(Suppl 24):1877–1878
  • Baysal E, Huisman THJ. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol. 1994;46(3):208–213
  • Desai SN, Colah RB. α-Thalassaemia syndromes in India. Indian J Hum Genet. 1997;3(1):1–9
  • Gupta RB, Tiwary RS, Pande PL, et al. Hemoglobinopathies among the Gond tribal groups of Central India; interaction of α- and β-thalassemia with β chain variants. Hemoglobin. 1991;15(5):441–458
  • Bernini L. Geographic distribution of α-thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, Eds. Disorders of Hemoglobin Genetics, Pathophysiology, and Clinical Management, 1st ed. New York, NY, USA: Cambridge University Press. 2001:878–894
  • Flint J, Harding RM, Clegg JB, et al. Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants. Hum Genet. 1993;91(2):91–117
  • Flint J, Harding RM, Boyce AJ, et al. The population genetics of the haemoglobinopathies. Bailliéres Clin Haematol. 1993;6(1):215–262
  • Fodde R, Losekoot M, van den Broek MH, et al. Prevalence and molecular heterogeneity of α+ thalassemia in two tribal populations from Andhra Pradesh, India. Hum Genet. 1988;80(2):157–160
  • Modiano G, Morpurgo G, Terrenato L, et al. Protection against malaria morbidity: Near-fixation of the α-thalassemia gene in a Nepalese population. Am J Hum Genet. 1991;48(2):390–397
  • Weatherall DJ. Genetic variation and susceptibility to infection: The red cell and malaria. Br J Haematol. 2008;141(3):276–286
  • Mukherjee M, Lu CY, Ducrocq R, et al. Effect of α-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India. Am J Hematol. 1997;55(2):104–109
  • Nadkarni A, Gorakshakar A, Lu C, et al. Molecular pathogenesis and clinical variability of β-thalassemia syndromes among Indians. Am J Hematol. 2001;68(2):75–80
  • Kanavakis E, Wainscoat JS, Wood WG, et al. The interaction of α thalassaemia with heterozygous β thalassaemia. Br J Haematol. 1982;52(3):465–473
  • Steinberg MH, Embury SH. α-Thalassemia in blacks: Genetic and clinical aspects and interactions with the sickle hemoglobin gene. Blood. 1986;68(5):985–990
  • Thein SL. Genetic modifiers of the β-haemoglobinopathies. Br J Haematol. 2008;141(3):357–366
  • Peters AL, van Noorden CJF. Glucose-6-phosphate dehydrogenase deficiency and malaria: Cytochemical detection of heterozygous G6PD deficiency in women. J Histochem Cytochem. 2009;57(11):1003–1011
  • Mukherjee MB, Colah RB, Martin S, Ghosh K. Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India – Country scenario. Indian J Med Res. 2015;141(5):516–520
  • Heller P, Best WR, Nelson RB, Becktel J. Clinical implications of sickle-cell trait and glucose-6-phosphate dehydrogenase deficiency in hospitalized Black male patients. N Engl J Med. 1979;300(18):1001–1005
  • Ulrich B, Olughbeimro S, Effiong CE, Luzzatto L. Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: Frequency and features of association in an African community. Blood. 1975;46(4):571–597

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