Molecular Aspects of Glucose-6-Phosphate Dehydrogenase Deficiency in Iran

Author(s):
Ali DehghanifardAli Dehghanifard1, Yousef MortazaviYousef Mortazavi1,*, Najmaldin SakiNajmaldin Saki2, Majid Farshdusti-HaghMajid Farshdusti-Hagh3
1Department of Pathology, Zanjan University of Medical Sciences, Zanjan, Iran
2Department of Hematology, Thalassemia and Hemoglobinopathy Research Center, Jundi Shapur University of Medical Sciences, Ahvaz, Iran
3Department of Hematology, Division of Laboratory Hematology and Blood Banking, Tabriz University of Medical Sciences, Tabriz, Iran
*Corresponding Author: Department of Pathology, Zanjan University of Medical Sciences, Zanjan, Iran Email: [email protected]

Zahedan Journal of Research in Medical Sciences:Vol. 14, issue 7; e93302
Published online:Jan 07, 2012
Article type:Review Article
Received:Aug 27, 2011
Accepted:Nov 16, 2011
How to Cite:Dehghanifard A, Mortazavi Y, Saki N, Farshdusti-Hagh M. Molecular Aspects of Glucose-6-Phosphate Dehydrogenase Deficiency in Iran. Zahedan J Res Med Sci. 2012;14(7):e93302. doi:

Abstract

Background: G6PD deficiency is the most common hereditary enzyme deficiency that affected more than 400 million people worldwide. This enzyme deficiency is caused by a spectrum of mutations in the gene encoding G6PD on chromosome X. Epidemiologically G6PD deficiency has been specially considered in Middle East countries including Iran, Oman and Saudi Arabia.
Materials and Methods: This study has reviewed more than 70 papers related to the epidemiological significance and various diagnostic strategies of G6PD deficiency from 1956 to 2010.
Results: The results showed a higher prevalence of Mediterranean variant followed by Chatham and Cosenza compared to other variants in Iran.
Conclusion: Accurate identification of G6PD deficiency variants in areas with high prevalence of this disease will help to screen patients and their families with risk level when faced with oxidant agents.

Fulltext

The full text of this article is available on the PDF file.

References

  • 1.
    The References of this article are available on the PDF file.

Copyright

© 2012, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Similar Articles

27
Jun
2011

The Prevalence of Mediterranean Mutation of Glucose-6-Phosphate Dehydrogenase (G6PD) in Zahedan

Alireza Nakhaee (Biochemistry),
Saeedeh Salimi,
Azita Zadehvakili,
Soroush Dabiri,
Mehrangiz Noora,
Mahnaz Rezaei
,et al.

Nakhaee (Biochemistry) A, Salimi S, Zadehvakili A, Dabiri S, Noora M, et al. The Prevalence of Mediterranean Mutation of Glucose-6-Phosphate Dehydrogenase (G6PD) in Zahedan. Zahedan J Res Med Sci. 2012;14(3):e93563. doi:

13
Sep
2009

Survey of the Prevalence of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Admitted Men for Premarriage Tests in Zahedan-Iran Reference Laboratory

Alireza Nakhaee (Biochemistry),
Soroush Dabiri,
Mehrangiz Noora

Nakhaee (Biochemistry) A, Dabiri S, Noora M. Survey of the Prevalence of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Admitted Men for Premarriage Tests in Zahedan-Iran Reference Laboratory. Zahedan J Res Med Sci. 2009;11(3):e94392. doi:

31
Aug
2017

Association of Serum Zinc Level with Severity of Acute Hemolysis in Iranian Children with Glucose-6-Phosphate Dehydrogenase Deficiency

Naser Honar,
Forough Saki,
Azadeh Rezaeefard,
Mahdi Shahriari

Honar N, Saki F, Rezaeefard A, Shahriari M. Association of Serum Zinc Level with Severity of Acute Hemolysis in Iranian Children with Glucose-6-Phosphate Dehydrogenase Deficiency. J Compr Ped. 2017;8(3):e55098. doi: https://doi.org/10.5812/compreped.55098

31
Mar
2004

Investigation of glucose-6-phosphate dehydrogenase deficiency by NADP test in jaundiced newborn‌

M Nobahar,
AA Vafaei

Nobahar M, Vafaei A. Investigation of glucose-6-phosphate dehydrogenase deficiency by NADP test in jaundiced newborn‌. J Inflamm Dis. 2024;7(5):e155006. doi:

15
Sep
2013

Prevalence of G6PD Deficiency in Neonatal Sepsis in Iran

Soheila Zareifar,
Narjes Pishva Pishva,
Mohamadreza Farahmandfar,
Shahab Benaei,
Nader Cohan

Zareifar S, Pishva NP, Farahmandfar M, Benaei S, Cohan N. Prevalence of G6PD Deficiency in Neonatal Sepsis in Iran. Inn J Pediatr. 2014;24(1):. doi:

Download PDF142.65 KB
Share on
Cited by
Metrics

Ordering Reprints

Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC 

Search Relations

Author(s):

Related Articles