syndrome

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Related to Crigler-Najjar syndrome: Dubin Johnson syndrome
References in periodicals archive ?
Pregnancy outcome in maternal Crigler-Najjar syndrome type II: A case report and systematic review of the literature.
Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II.
Identification of defect in the genes for bilirubin UDP-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type II.
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.
Strom's group also used the liver cells to correct liver function in an 11-year-old child with Crigler-Najjar syndrome, an inherited liver disease in which a missing enzyme affects the liver's ability to process bilirubin, leading to jaundice.
today announced that researchers at the University of Minnesota (Minneapolis) and Albert Einstein College of Medicine (New York) have utilized the Company's gene repair technology, termed chimeraplasty, to permanently correct a gene defect in the Gunn rat model of Crigler-Najjar syndrome type I.