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KMID : 0381219740060040219
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Journal of RIMSK
1974 Volume.6 No. 4 p.219 ~ p.222
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One Case of Gilbest´s Syndrome with Hemochromatosis
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Abstract
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Gilbert´s syndrome is a relatively rare syndrome characterized by chronic, benign, intermittent jaundice without hemolysis which associated with a retention of unconjugated bilirubin in the plasma and familial tendency. The criteria for diagnosis are as follows: an unconjugated hyper
bilirubinemia on at least two occasions over a period of six months, with normal concentrations of serum conjugated bilirubin; scleral icterus as the only abnormal physical finding; and normal results for serum trasaminase and alkaline phosphatase activities, hepatic histology by light microscopy, hemoglobin concentration, peripheral blood smear, white-cell count, reticulocyte count on at least two occasions and red-cell osmotic fragility.
Recently we observed a case considered as Gilbert´s syndrome in the Department of Internal Medicine, Catholic Medical College, who was a 21 years old student with chronic, benign, unchonjugated hyperbilirubinemia without hemolysis. We report this case and review the literatures.
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KEYWORD
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