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Hemoglobin
international journal for hemoglobin research
Volume 44, 2020 - Issue 5
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Brief Report

Identification and Development of a High-Risk District Model in the Prevention of β-Thalassemia in Telangana State, India

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Pages 371-375 | Received 21 Mar 2020, Accepted 13 Aug 2020, Published online: 02 Oct 2020

References

  • Koren A, Lora P, Luci Z, et al. Prevention of β thalassemia in Northern Israel – a cost-benefit analysis. Mediterr J Hematol Infect Dis. 2014;6(1):e2014022.
  • Madan N, Sharma S, Sood S, et al. Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India. Indian J Hum Genet. 2010;16(1):16–25.
  • Mohanty D, Colah RB, Gorakshakar AC, et al. Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicenter study. J Community Genet. 2013;4(1):33–42.
  • Sharma RS, Parckh JG, Shah KM. Hemoglobinopathies in western India. J Assoc Physicians India. 1963;11:969–973.
  • Sukumaran PK. Abnormal hemoglobins in India. In: Sen NN, Basu AK, editors. Trends in hematology. Calcutta (India): Saraswati Press; 1975. p. 225–236.
  • Dash S. Beta-thalassaemia trait in the Punjab (North India). Br J Haematol. 1985;61(1):185–186.
  • Rao VR, Gorakshakar AC. Sickle cell hemoglobin, beta-thalassemia and G6PD deficiency in tribes of Maharashtra. Gene Geogr. 1990;4(3):131–134.
  • Misra RC, Ram B, Mohapatra BC. High prevalence & heterogeneity of thalassemias in Orissa. Indian J Med Res. 1991;94:391–394.
  • Balgir RS. Genetic epidemiology of the three predominant abnormal hemoglobins in India. J Assoc. Phyisicians India. 1996;44(1):25–28.
  • Balgir RS. Spectrum of hemoglobinopathies in the State of Orissa, India: a ten years cohort study. J Assoc Physicians India. 2005;53:1021–1026.
  • Jawahirani A, Mamtani M, Das K, et al. Prevalence of beta-thalassaemia in subcastes of Indian Sindhis: results from a two-phase survey. Public Health. 2007;121(3):193–198.
  • Dolai TK, Dutta S, Bhattacharyya M, et al. Prevalence of hemoglobinopathies in rural Bengal, India. Hemoglobin. 2012;36(1):57–63.
  • Patel AP, Naik MR, Shah NM, et al. Prevalence of common hemoglobinopathies in Gujarat: an analysis of a large population screening program. Nat J Community Med. 2012;3(1):112–116.
  • Colah R, Italia K, Gorakshakar A. Burden of thalassemia in India: the road map for control. J Pediatr Haematol Oncol. 2017;2(4):79–84.
  • Colah R, Gorakshakar A, Phanasgaonkar S, et al. Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. Br J Haematol. 2010;149(5):739–747.
  • Trehan A, Sharma N, Das R, et al. Clinicoinvestigational and demographic profile of children with thalassemia major. Indian J Hematol Blood Transfus. 2015;31(1):121–126.
  • Kosaryan M, Karami H, Darvishi-Khezri H, et al. Demographic data of patients with β-thalassemia major recorded in the electronic system in the north of Iran. Tanzania J Health Res. 2016;20(3):1–7.
  • Majumder PP, Malhotra KC. Matrimonial distance, inbreeding coefficient and population size: Dhangar data. Ann Hum Biol. 1979;6(1):17–27.
  • Rao VR. Gond ethnic milieu and the extent of an endogamous group: Naik Gonds. J Ind Anth Soc. 1988;23(1):57–62.
  • Waldman MR, Zeghal M. Islamic world: migration and renewal (1041–1405). Chicago (IL): Encyclopedia Britannica; 2019. Available from: https://www.britannica.com/topic/Islamic-world
  • Suresh Lal B. A historical study of origin and migration of Banjara tribe in Telangana State. Int J Curr Res. 2016;8(10):40261–40267.
  • Chawla S, Singh RK, Lakkakula BVKS, et al. Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India. J Community Genet. 2017;8(3):159–166.
  • Mehta BC, Dave VB, Joshi SR. Study of hematological and genetic characteristics of Cutchi Bhanushali community. Indian J Med Res. 1972;60(2):305–311.
  • Bhatia HM, Shanbagh SR, Baxi AJ, et al. Genetic studies among the endogamous groups of Lohanas of North and West India. Hum Hered. 1976;26(4):298–305.
  • Mulchandani DV, Fulare MB, Zodpey SP, et al. Prevalence of some epidemiological factors of β-thalassemia trait in Sindhi community of Nagpur City, India. Indian J Pub Health. 2008;52(1):11–15.
  • Prevention and control of hemoglobinopathies in India – beta thalassemia, sickle cell disease and other variant haemoglobins: National Health Mission Guidelines on Hemoglobinopathies in India. New Delhi (India): Ministry of Health and Family Welfare, Government of India; 2018.
  • Karve I. Hindu society: an interpretation. Menlo Park (CA): Benjamin/Cummings Publishing Co; 1978.

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