December 3, 2024
G6PD trait: societal importance to ensure well-being of female heterozygotes for health and childbirth
  • Beutler, E. G6PD deficiency. Blood 84, 3613–3636 (1994).

    Article 
    CAS 
    PubMed 

    Google Scholar 

  • Herschel, M. & Beutler, E. Low glucose-6-phosphate dehydrogenase enzyme activity level at the time of hemolysis in a male neonate with the African type of deficiency. Blood Cells Mol. Dis. 27, 918–923 (2001).

    Article 
    CAS 
    PubMed 

    Google Scholar 

  • Kaplan, M., Hammerman, C. & Bhutani, V. K. Parental education and the WHO neonatal G-6-PD screening program: a quarter century later. J. Perinatol. 35, 779–784 (2015).

    Article 
    CAS 
    PubMed 

    Google Scholar 

  • Kaplan, M., Wong, R. J. & Stevenson, D. K. Hemolysis and glucose-6-phosphate dehydrogenase deficiency-related neonatal hyperbilirubinemia. Neonatology 114, 223–225 (2018).

    Article 
    CAS 
    PubMed 

    Google Scholar 

  • Watchko, J. F. et al. Should we screen newborns for glucose-6-phosphate dehydrogenase deficiency in the United States? J. Perinatol. 33, 499–504 (2013).

    Article 
    CAS 
    PubMed 

    Google Scholar 

  • Kaplan M., Kassirer Y. & Hammerman C. Controversies in our understanding of extreme hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient neonates. Pediatr. Res. (2024).

  • GBD 2021 Diseases and Injuries Collaborators. Global incidence, prevalence, years lived with disability (YLDs), disability-adjusted life-years (DALYs), and healthy life expectancy (HALE) for 371 diseases and injuries in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet 403, 2133–2161 (2024).

    Article 

    Google Scholar 

  • Bhutani, V. K. et al. Neonatal hyperbilirubinemia and Rhesus disease of the newborn: incidence and impairment estimates for 2010 at regional and global levels. Pediatr. Res. 74, 86–100 (2013).

    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Bhutani, V. K., Vidavalur, R. & Wong, R. J. Advances to diminish global newborn kernicterus mortality. J. Perinatol. 44, 493–500 (2024).

    Article 
    PubMed 

    Google Scholar 

  • Howes, R. E. et al. G6PD deficiency prevalence and estimates of affected populations in malaria endemic countries: a geostatistical model-based map. PLoS Med. 9, e1001339 (2012).

    Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Padilla, C. D. & Therrell, B. L. Newborn screening in the Asia Pacific region. J. Inherit. Metab. Dis. 30, 490–506 (2007).

    Article 
    PubMed 

    Google Scholar 

  • Pfeffer, D. A. et al. Genetic variants of glucose-6-phosphate dehydrogenase and their associated enzyme activity: a systematic review and meta-analysis. Pathogens 11, 1045 (2022).

    Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Au, W. Y. et al. Glucose 6-phosphate dehydrogenase (G6PD) deficiency in elderly Chinese women heterozygous for G6PD variants. Am. J. Med Genet A. 129A, 208–211 (2004).

    Article 
    PubMed 

    Google Scholar 

  • Kemper, A. R. et al. Clinical practice guideline revision: management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics 150, e2022058859 (2022).

    Article 
    PubMed 

    Google Scholar 

  • Milburn, S. et al. Implementation of universal screening for G6PD deficiency in newborns. Pediatrics 154, e2024065900 (2024).

    Article 
    PubMed 

    Google Scholar 

  • WHO Working Group. Glucose-6-phosphate dehydrogenase deficiency. Bull. World Health Organ. 67, 601–611 (1989).

    Google Scholar 

  • link

    Leave a Reply

    Your email address will not be published. Required fields are marked *