194
Views
0
CrossRef citations to date
0
Altmetric
Hematology

Molecular Detection of Hemoglobin O-Arab in the Sudanese Population

ORCID Icon & ORCID Icon
Pages 3323-3330 | Received 03 Jun 2023, Accepted 28 Jul 2023, Published online: 03 Aug 2023

References

  • Victor Hoffbrand A, Catovsky D, Edward GD. Postgraduate haematology. 5th ed. Tuddenham: Wiley; 2008.
  • Hoffbrand AV, Moss PAH, Pettit JE. Essential Hematology. 5th ed. UK: Wiley Black wel; 2006.
  • William F, Kern MD. PDQ Hematology. 1st ed. US: PMPH; 2002.
  • Papadopoulos V. The implications of hemoglobin O-Arab mutation. Haematologica. 2003; 2003:1.
  • Merck KG. Sanger sequencing steps & method: Germany; 2021.
  • Untergasser A, Cutcutache I, Koressaar T, et al. Primer3-new capabilities and interfaces. Nucleic Acids Res. 2012;40(15):e115. doi:10.1093/nar/gks596
  • Altschul SF, Gish W, Miller W, Myers E, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;215:403–410. doi:10.1016/S0022-2836(05)80360-2
  • Khalafallah TO, Ajab Eldoor AA, Babker AM, et al. Hematological and molecular analyses of the HbS allele among the Sudanese population. J Int Med Res. 2022;50(9):3000605221125050. PMID: 36134571; PMCID: PMC9502246. doi:10.1177/03000605221125050
  • Ibrahim SA, Mustafa D. Sickle-cell haemoglobin O disease in a Sudanese family. Br Med J. 1967;3(5567):715–717. PMID: 6038366; PMCID: PMC1843069. doi:10.1136/bmj.3.5567.715
  • Vella F, Beale D, Lehmann H. Haemoglobin O Arab in Sudanese. Nature. 1966;209(5020):308–309. PMID: 5915974. doi:10.1038/209308a0
  • ElHazmi MAF, Lehmann H. Human haemoglobins and haemoglobinopathies in Arabia: Hb O Arab in Saudi Arabia. Acta Haematol. 1980;63:268–273. doi:10.1159/000207414
  • Zimmerman SA, O’Branski EE, Rosse WF, Ware RE. Hemoglobin S/O (Arab): thirteen new cases and review of the literature. Am J Hematol. 1999;60:279–284. doi:10.1002/(SICI)1096-8652(199904)60:4<279::AID-AJH5>3.0.CO;2-2
  • Sangare A, Sanogo I, Meite M, et al. L’hémoglobine o Arab en Côte d’Ivoire et en Afrique de l’Ouest [Hemoglobin O Arab in Ivory Coast and western Africa]. Med Trop. 1992;52(2):163–167. French. PMID: 1328806.
  • Ata F, Rahhal A, Malkawi L, et al. Genotypic and phenotypic composition of sickle cell disease in the Arab population - a systematic review. Pharmgenomics Pers Med. 2023;16:133–144. PMID: 36851992; PMCID: PMC9961577. doi:10.2147/PGPM.S391394
  • Collins Nwabuko O, Eke R, Jean Claude Kazadi M. Beyond the legislation for sickle cell disease prevention - getting the right outcomes. Am J Intern Med. 2019;7(3):56–65. doi:10.11648/j.ajim.20190703.12
  • Qua K, Swiatkowski SM, Gurkan UA, Pelfrey CM. A retrospective case study of successful translational research: gazelle Hb variant point-of-care diagnostic device for sickle cell disease. J Clin Transl Sci. 2021;5(1):e207. doi:10.1017/cts.2021.871