ALLMedicine Unconjugated Hyperbilirubinemia Center

May 22nd, 2020 - Neonatal hyperbilirubinemia is a common condition that frequently requires treatment with phototherapy and less commonly by exchange transfusion, especially in preterm infants. It is important to identify and monitor infants at risk of severe unco...

May 1st, 2020 - Unconjugated hyperbilirubinemia, a feature of neonatal jaundice or Crigler-Najjar syndrome, can lead to neurotoxicity and even death. We previously demonstrated that unconjugated bilirubin (UCB) can be eliminated via transintestinal excretion in G...

Feb 12th, 2020 - Mild hemolysis is difficult to determinate by traditional methods, and its role in Gilbert's syndrome (GS) is unclear. The main aims were to inspect the erythrocyte (RBC) survival in GS by using Levitt's carbon monoxide (CO) breath test and to ass...

Dec 20th, 2019 - Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.|2019|Kim JJ,Oh J,Kim Y,Lee KA,|genetics,genetics,diagnosis,genetics,

Sep 9th, 2019 - Crigler-Najjar syndrome (CNS) results from biallelic mutations of UGT1A1 causing partial or total loss of uridine 5'-diphosphate glucuronyltransferase activity leading to unconjugated hyperbilirubinemia and its attendant risk for irreversible neur...

May 22nd, 2020 - Neonatal hyperbilirubinemia is a common condition that frequently requires treatment with phototherapy and less commonly by exchange transfusion, especially in preterm infants. It is important to identify and monitor infants at risk of severe unco...

May 1st, 2020 - Unconjugated hyperbilirubinemia, a feature of neonatal jaundice or Crigler-Najjar syndrome, can lead to neurotoxicity and even death. We previously demonstrated that unconjugated bilirubin (UCB) can be eliminated via transintestinal excretion in G...

Feb 12th, 2020 - Mild hemolysis is difficult to determinate by traditional methods, and its role in Gilbert's syndrome (GS) is unclear. The main aims were to inspect the erythrocyte (RBC) survival in GS by using Levitt's carbon monoxide (CO) breath test and to ass...

Dec 20th, 2019 - Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.|2019|Kim JJ,Oh J,Kim Y,Lee KA,|genetics,genetics,diagnosis,genetics,

Sep 9th, 2019 - Crigler-Najjar syndrome (CNS) results from biallelic mutations of UGT1A1 causing partial or total loss of uridine 5'-diphosphate glucuronyltransferase activity leading to unconjugated hyperbilirubinemia and its attendant risk for irreversible neur...

Abstract and Introduction We report the coexistence of Gilbert's syndrome and homozygous sickle cell disease in a child with persistent unconjugated hyperbilirubinemia. Gilbert's syndrome is a common benign hereditary disorder of bilirubin metabol...