Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 44, 2020 - Issue 1
184
Views
5
CrossRef citations to date
0
Altmetric
Original Articles

Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma’ah, Saudi Arabia

ORCID Icon, , , , &
Pages 47-50 | Received 31 Oct 2019, Accepted 23 Jan 2020, Published online: 24 Feb 2020

References

  • Weatherall DJ. Hemoglobin and inherited disorders of globin synthesis. In: Hoffbrand AV, Catovsky D, Tuddenham EGD, Editors. Postgraduate Haematology, 5th ed. Oxford (Oxfordshire, UK): Blackwell Scientific Publication. 2005:85–90.
  • Rahimi Z. Genetic epidemiology, hematological and clinical features of hemoglobinopathies in Iran. Biomed Res Int. 2013;2013:1–10.
  • Clarke GM, Higgins TN. Laboratory investigation of hemoglobinopathies and thalassemias: review and update. Clin Chem. 2000;46(8):1284–1290.
  • Patel AP, Naik MR, Shah NM, et al. Prevalence of common hemoglobinopathies in Gujarat: an analysis of a large population screening programme. Natl J Community Med. 2012;3(1):112–116.
  • Mondal SK, Mandal S. Prevalence of thalassemia and hemoglobinopathy in eastern India: a 10-year high-performance liquid chromatography study of 119,336 cases. Asian J Transfus Sci. 2016;10(1):105–110.
  • Al-Awamy BH. Thalassemia syndromes in Saudi Arabia. Meta-analysis of local studies. Saudi Med J. 2000;21(1):8–17.
  • Rahimi Z, Muniz A, Parsian A. Detection of responsible mutations for β thalassemia in the Kermanshah Province of Iran using PCR-based techniques. Mol Biol Rep. 2010;37(1):149–154.
  • Africa Health Organization (AHO). Sickle-cell disease and other hemoglobin-disorders. Africa Health Organization; [cited 2020 Feb 3]. Available from: https://aho.org/fact-sheets/sickle-cell-disease-and-other-haemoglobin-disorders-fact-sheet/
  • Al-Gazali L, Hamamy H, Al-Arrayad S. Genetic disorders in the Arab world. Br Med J. 2006;333(7573):831–834.
  • El-Hazmi MA, Al-Hazmi AM, Warsy AS. Sickle cell disease in Middle East Arab countries. Indian J Med Res. 2011;134(5):597–610.
  • Warghade S, Britto J, Haryan R, et al. Prevalence of hemoglobin variants and hemoglobinopathies using cation-exchange high-performance liquid chromatography in central reference laboratory of India: a report of 65779 cases. J Lab Physicians. 2018;10(1):73–79.
  • Balgir RS. The genetic burden of hemoglobinopathies with special reference to community health in India and the challenges ahead. Indian J Hematol Blood Transfus. 2002;20:2–7.
  • El-Hazmi MA, Al-Swailem AR, Warsy AS, et al. Consanguinity among the Saudi Arabian population. J Med Genet. 1995;32(8):623–626.
  • Alhamdan NA, Almazrou YY, Alswaidi FM, et al. Premarital screening for thalassemia and sickle cell disease in Saudi Arabia. Genet Med. 2007;9(6):372–377.
  • Alswaidi FM, O'Brien SJ. Premarital screening programmes for hemoglobinopathies, HIV and hepatitis viruses: review and factors affecting their success. J Med Screen. 2009;16(1):22–28.
  • Meyer BF. Strategies for the prevention of hereditary diseases in a highly consanguineous population. Ann Hum Biol. 2005;32(2):174–179.
  • Karimi M, Jamalian N, Yarmohammadi H, et al. Premarital screening for β-thalassaemia in Southern Iran: options for improving the programme. J Med Screen. 2007;14(2):62–66.
  • Keskin A, Turk T, Polat A, et al. Premarital screening of β-thalassemia trait in the province of Denizli, Turkey. Acta Haematol. 2000;104(1):31–33.
  • Al-Arrayed S, Hafadh N, Al-Serafi S. Premarital counseling: an experience from Bahrain. East Mediterr Health J. 1997;3(3):415–419.
  • Jastaniah W. Epidemiology of sickle cell disease in Saudi Arabia. Ann Saudi Med. 2011;31(3):289–293.
  • Lehmann H, Maranjian G, Mourant AE. Distribution of sickle-cell hemoglobin in Saudi Arabia. Nature. 1963;198(4879):492–493.
  • Al-Qurashi MM, El-Mouzan MI, Al-Herbish AS, et al. The prevalence of sickle cell disease in Saudi children and adolescents. A community-based survey. Saudi Med J. 2008;29(10):1480–1483.
  • El-Hazmi MA, Warsy AS. Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia. East Mediterr Health J. 1999;5(6):1147–1153.
  • El-Hazmi MA. Clinical and haematological diversity of sickle cell disease in Saudi children. J Trop Pediatr. 1992;38(3):106–112.
  • Patne SC, Shukla J. Hemoglobin E disorders in Eastern Uttar Pradesh. Indian J Pathol Microbiol. 2009;52(1):110–112.
  • Al-Suliman A. Prevalence of β-thalassemia trait in premarital screening in Al-Hassa, Saudi Arabia. Ann Saudi Med. 2006;26(1):14–16.
  • Abu-Osba YK, Mallouh A, Salamah M, et al. Comprehensive newborn screening program: ARAMCO experience, the national need and recommendations. Ann Saudi Med. 1992;12(3):235–240.
  • Memish ZA, Saeedi MY. Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia. Ann Saudi Med. 2011;31(3):229–235.
  • Colah R, Gorakshakar A, Nadkarni A. Global burden, distribution and prevention of β-thalassemias and Hemoglobin E disorders. Expert Rev Hematol. 2010;3(1):103–117.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.