UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China

被引:0
作者
Hui Yang
Fen Lin
Zi-kai Chen
Lin Zhang
Jia-Xin Xu
Yong-Hao Wu
Jing-Ying Gu
Yu-Bin Ma
Jian-Dong Li
Li-Ye Yang
机构
[1] School of Medicine,Department of Laboratory Medicine
[2] Yangtze University,Central Laboratory
[3] Chaozhou Central Hospital Affiliated to Southern Medical University,Department of Pediatrics
[4] School of Food Engineering and Biotechnology,Lab for Respiratory Disease
[5] Hanshan Normal University,undefined
[6] Chaozhou Central Hospital Affiliated to Southern Medical University,undefined
[7] People’s Hospital of Yangjiang,undefined
来源
BMC Pediatrics | / 21卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 148 条
  • [1] Kaplan M(2011)Severe neonatal hyperbilirubinemia and kernicterus: are these still problems in the third millennium? Neonatology 100 354-362
  • [2] Bromiker R(2009)Visual assessment of jaundice in term and late preterm infants Arch Dis Child Fetal Neonatal Ed 94 F317-F322
  • [3] Hammerman C(1999)Frequency of neonatal bilirubin testing and hyperbilirubinemia in a large health maintenance organization Pediatrics 104 1198-1203
  • [4] Keren R(2001)Neonatal hyperbilirubinemia N Engl J Med 344 581-590
  • [5] Tremont K(2011)Risk assessment and follow-up are the keys to preventing severe hyperbilirubinemia J Pediatr 39 275-276
  • [6] Luan X(2004)Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation Pediatrics 114 297-316
  • [7] Cnaan A(1992)Neonatal jaundice in Asia Baillieres Clin Hematol 5 131-142
  • [8] Newman TB(2002)Understanding neonatal hyperbilirubinaemia in the era of genomics Semin Neonatol 7 143-152
  • [9] Escobar GJ(2000)Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype Hum Mutat 16 297-306
  • [10] Gonzales VM(2013)Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database Blood Cells Mol Dis 50 273-280