Glucose-6-phosphate dehydrogenase deficiency and severe neonatal hyperbilirubinemia: a complexity of interactions between genes and environment

Seminars in Fetal & Neonatal Medicine
Michael Kaplan, C Hammerman

Abstract

Glucose-6-phosphate dehydrogenase deficiency is a commonly occurring genetic condition, likely to be encountered today in virtually any corner of the globe. Sudden episodes of hemolysis associated with the condition may result in exponential increases in serum total bilirubin concentrations to levels at which bilirubin-induced neurologic damage may occur. The hyperbilirubinemia is the result of complex interactions between genes and environment. Neonatal screening programs coupled with parental and medical caretaker education may be successful in limiting the severity of disease.

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Citations

Oct 7, 2014·Seminars in Perinatology·Michael KaplanCathy Hammerman
Jun 28, 2013·Journal of Perinatology : Official Journal of the California Perinatal Association·V NairK Yusuf
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Mar 9, 2010·Seminars in Perinatology·David S MillingtonVamsee Pamula
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Dec 15, 2020·Seminars in Perinatology·Lizhong DuVinod K Bhutani
Dec 5, 2012·Pediatrics·Patrizia ZaramellaLino Chiandetti

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