单词 | gilbert syndrome |
释义 | Gilbert syndromefa·mil·i·al non·he·mo·lyt·ic jaun·dice[MIM*143500]Gilbert syndromeA benign hereditary condition (OMIM:143500) in which reduced bilirubin transferase activity results in intermittent hyperbilirubinaemia.Gilbert syndromeConstitutional liver dysfunction, low-grade chronic hyperbilirubinemia An inherited defect in bilirubin metabolism Clinical Jaundice, weakness, fatigue, nausea, abdominal pain. Cf Criggler-Najjar disease.Gilbert,Nicholas A., French physician, 1858-1927. |
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