Crigler-Najjar syndrome type 1

Crigler-Najjar syndrome type 1 (CNS1) is the most severe form of CNS, a hereditary disorder of hepatic bilirubin conjugation, characterized by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic bilirubin glucuronosyltransferase (BGT).

Also known as: Crigler-Najjar syndrome, type 1, Crigler-Najjar syndrome, type I, UGT deficiency type 1, bilirubin uridinediphosphate glucuronosyltransferase deficiency type 1, bilirubin-UGT deficiency type 1, hereditary unconjugated hyperbilirubinemia type 1, hyperbilirubinemia, Crigler-Najjar type 1, Crigler Najjar syndrome, type 1

0 clinical trials for this condition and its sub-types, 0 tagged with Crigler-Najjar syndrome type 1 itself.