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- W498542364 abstract "Crigler-Najjar syndrome (CNS) is a rare disorder of bilirubin metabolism caused by the lack or deficiency of the enzyme uridine diphosphate (UDP)- glucuronosyltransferase (UGT). A 2-month-old girl here presented with prolonged jaundice was diagnosed with CNS Type 1 and had been treated by phototherapy. Final diagnose was made after excluding other more common causes of unconjugated hyperbilirubinemia, reviewing the clinical course and response to phenobarbital. Accurate diagnosis of Crigler-Najjar syndrome is important because of the implications for prognosis and treatment. Treatment of CNS Tip 1 consists of the aggressive use of measures to remove bilirubin ( either phototherapy or exchange transfusion), while liver transplantation is the definitive treatment" @default.
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- W498542364 date "2002-03-01" @default.
- W498542364 modified "2023-09-24" @default.
- W498542364 title "Prolonged unconjugated hyperbilirubinemia associated with Crigler-Najjar type 1 syndrome: Case report" @default.
- W498542364 doi "https://doi.org/10.16948/zktb.90803" @default.
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