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Definition of Gilbert syndrome

Gilbert syndrome: A common but harmless genetic condition in which UDP-glucuronosyltransferase, a liver enzyme that is essential to the disposal of bilirubin, is abnormal. Mutations in the same gene cause the Crigler-Najjar syndrome, which is a more severe and dangerous form of hyperbilirubinemia (high bilirubin in the blood). Also known as hyperbilirubinemia type 1.

Source: MedTerms™ Medical Dictionary
http://www.medicinenet.com/script/main/art.asp?articlekey=7411
Last Editorial Review: 3/19/2012

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