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G6PD deficiency and Harilaou variant in a newborn: Intrauterine haemolysis and meconium aspiration syndrome Cover

G6PD deficiency and Harilaou variant in a newborn: Intrauterine haemolysis and meconium aspiration syndrome

Open Access
|Oct 2021

References

  1. Ntaios G, Chatzinikolaou A, Tomos C, Manolopoulos C, Karalazou P, Nikolaidou A, et al. Prevalence of glucose-6-phosphate dehydrogenase deficiency in Northern Greece. Intern Med J. 2008;38(3):204-6. doi: 10.1111/j.1445-5994.2007.01618.x.
  2. Missiou-Tsagaraki S. Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: prevalence among 1,286,000 Greek newborn infants. J Pediatr. 1991;119(2):293-9. doi: 10.1016/s0022-3476(05)80747-4.
  3. Bulliamy T, Luzzatto L, Hirono A, Beutler E. Hematologically important mutations: glucose-6-phosphate dehydrogenase. Blood Cells Mol Dis. 1997;23(2):302-13. doi: 10.1006/bcmd.1997.0147.
  4. Vives-Corrons JL, Kuhl W, Pujades MA, Beutler E. Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361A. Am J Hum Genet. 1990;47(3):575-9.
  5. Nkhoma ET, Poole C, Vannappagari V, Hall SA, Beutler E. The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis. Blood Cells Mol Dis. 2009;42(3):267-78. doi: 10.1016/j.bcmd.2008.12.005.
  6. Town M, Athanasiou-Metaxa M, Luzzatto L. Intragenic interspecific complementation of glucose 6-phosphate dehydrogenase in human-hamster cell hybrids. Somat Cell Mol Genet. 1990;16(2):97-108. doi: 10.1007/BF01233040.
  7. Fenton TR, Kim JH. A systematic review and meta-analysis to revise the Fenton growth chart for preterm infants. BMC Pediatr. 2013;13:59. doi: 10.1186/1471-2431-13-59.
  8. Keller CC, Joosten M, Middeldorp AM, Knapen MF. Fetal anemia caused by the Guadalajara variant of G6PD deficiency. Prenat Diagn. 2015;35(12):1255-7. doi: 10.1002/pd.4677.
  9. Choudhury SN, Kumar B, Saji PN. A Study of meconium aspiration syndrome and neonatal outcome: a prospective study. J Med Sci Clin Res. 2020;8(6):226-231. doi: 10.18535/jmscr/v8i6.41.
  10. Lindenskov PH, Castellheim A, Saugstad OD, Mollnes TE. Meconium aspiration syndrome: possible pathophysiological mechanisms and future potential therapies. Neonatology. 2015;107(3):225-30. doi: 10.1159/000369373.
  11. Poggi V, Town M, Foulkes NS, Luzzatto L. Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA. Biochem J. 1990;271(1):157-60. doi: 10.1042/bj2710157.
  12. Davidson R, Nitowsky H, Childs B. Demonstration of two populations of cells in the human female heterozygous for glucose-6-phosphate dehydrogenase variants. Proc Natl Acad Sci U S A. 1963;50(3):481-5. doi: 10.1073/pnas.50.3.481.
DOI: https://doi.org/10.34763/jmotherandchild.20212501.d-20-00021 | Journal eISSN: 2719-535X | Journal ISSN: 2719-6488
Language: English
Page range: 61 - 64
Submitted on: Dec 17, 2020
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Accepted on: Mar 25, 2021
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Published on: Oct 11, 2021
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2021 Kleoniki I. Athanasiadou, Maria Amarantidou, Eftychia Drogouti, Marina Economou, George Mitsiakos, Evgenia Papakonstantinou, Paraskevi Karagianni, published by Institute of Mother and Child
This work is licensed under the Creative Commons Attribution 4.0 License.