Vol. 3 No. 1 (2020)

  • Open Access

    Article

    Article ID: 166

    Advances in studies on the polymorphism of UGT1A1 gene in neonates with unexplained hyperbilirubinemia

    by Meiling Hu

    Insight - Chinese Medicine, Vol.3, No.1, 2020; 858 Views, 20 PDF Downloads

    DOI: https://doi.org/10.18282/i-cm.v3i1.166

    Neonatal hyperbilirubinemia is a common clinical symptom in the neonatal period. Severe jaundice can cause neonatal bilirubin encephalopathy. Clinically because severe hyperbilirubinemia more causes, the cause of hemolysis and infection is more common, this also accounted for a certain proportion of unknown reasons. UGT1A1 is a key enzyme for bilirubin metabolism, and unexplained jaundice is associated with a decrease in UGT1A1 activity caused by mutations in UGT1A1 gene, leading to neonatal persistent jaundice. The relationship between neonatal unexplained hyperbilirubinemia and UGT1A1 gene polymorphism was reviewed.