Glucose-6-Phosphate Dehydrogenase Deficiency: A Worldwide Potential Cause of Severe Neonatal Hyperbilirubinemia
Author:
Affiliation:
1. Department of Neonatology, Shaare Zedek Medical Center; Faculty of Medicine of the Hebrew University, Jerusalem, Israel.
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Link
https://publications.aap.org/neoreviews/article-pdf/1/2/e32/878963/e32.pdf
Reference26 articles.
1. Bancroft JD, Kreamer B, Gourley GR. Gilbert syndrome accelerates development of neonatal jaundice. J Pediatr. 1998;132:656-660
2. Beutler E. G6PD deficiency. Blood. 1994;84:3613-3636
3. Beutler E, Blume KG, Kaplan JC, Lohr GW, Ramot B, Valentine WN. International Committee for Standardization in Haematology: recommended screening test for glucose-6-phosphate dehydrogenase deficiency. Br J Haematol. 1979;43:469-477
4. Bosma PJ, Chowdhury JR, Bakker C, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyl transferase 1 in Gilbert’s syndrome. N Engl J Med. 1995;333:1171-1175
5. Bhutani VK, Johnson L, Sivieri EM. Predictive ability of a predischarge hour-specific serum bilirubin for subsequent signficant hyperbilirubinemia in healthy term and near-term newborns. Pediatrics. 1999;103:6-14
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1. Glucose-6-Phosphate Dehydrogenase Deficiency and Borderline Deficiency: Association with Neonatal Hyperbilirubinemia;The Journal of Pediatrics;2012-08
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3. Hyperbilirubinemia;Critical Care Nursing Clinics of North America;2009-03
4. Donor Blood Glucose 6-Phosphate Dehydrogenase Deficiency Reduces the Efficacy of Exchange Transfusion in Neonatal Hyperbilirubinemia;Pediatrics;2009-01-01
5. Hyperbilirubinemia in term and near-term infants: Kernicterus on the rise?;Newborn and Infant Nursing Reviews;2004-12
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