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Barkha Goswami

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From Childhood Icterus to Adolescent Gallstones: Clinically Diagnosed Crigler‐Najjar Syndrome Type II

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By Danish Kumar Goswami, Barkha Goswami, Samiullah Shaikh
| Wiley Online Library Verified
1 Introduction Crigler–Najjar syndrome (CNS) is a rare autosomal recessive disorder of bilirubin metabolism caused by mutations in the uridine diphosphate-glucuronosyltransferase (UGT1A1) gene, leading to reduced or absent activity of the hepatic enzyme UGT1A1, thus resulting in unconjugated hyperbilirubinemia of varying severity.
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