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European journal of pediatrics, 2012
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. In patients with Gilbert syndrome, uridine diphosphate-glucuronyl transferase activity is reduced to 30% of the normal, resulting in ...
Andrew, Fretzayas +3 more
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Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. In patients with Gilbert syndrome, uridine diphosphate-glucuronyl transferase activity is reduced to 30% of the normal, resulting in ...
Andrew, Fretzayas +3 more
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Gilbert's Syndrome—Does It Exist?
Acta Medica Scandinavica, 1988Abstract. Liver function tests and prevalence of different symptoms generally said to occur in Gilbert's syndrome were analysed in male conscripts and in male and female participants in two cross‐sectional population studies in Göteborg, in total 2395 subjects. The serum bilirubin levels showed a skew distribution without bimodality.
R, Olsson +6 more
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UDP-Glucuronosyltransferase in gilbert’s syndrome
Pathology, 1996The diagnosis of Gilbert's syndrome, a condition characterised by mild jaundice related to chronic unconjugated hyperbilirubinemia, is often presumptive and the pathogenesis is incompletely understood. It would be of interest to develop an immunohistochemical staining method to confirm a diagnosis of Gilbert's syndrome.
H S, Debinski +5 more
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Evaluation of Tests for Gilbert's Syndrome
Acta Medica Scandinavica, 1980ABSTRACT. The effect of caloric restriction (400 kcal for 24 hours) on serum total and unconjugated bilirubin was studied in 30 subjects with Gilbert's syndrome and in 22 patients with different liver diseases. The method could not completely differentiate between Gilbert's syndrome and liver disease, but an increase in unconjugated bilirubin of 15 ...
R, Olsson, G, Lindstedt
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TREATMENT OF GILBERT'S SYNDROME WITH PHENOBARBITONE
The Lancet, 1970Abstract Thirteen patients with Gilbert's syndrome have been treated with phenobarbitone. In all instances there was a rapid fall in the plasma-bilirubin, and in three of the ten symptomatic patients the symptoms improved. The reduction in the plasma-bilirubin was associated with, and thought to be the result of, an increase in hepatic bilirubin U.D.P.
M, Black, S, Sherlock
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A Case of Acquired Gilbert’s Syndrome
Clinical Pediatrics, 2016Leong, Jonathan, Serrano, Maria-Stella
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