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Gilbert's Syndrome

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Description: Information includes description, enzyme defect, clinical and laboratory findings, diagnosis, and treatment.
Gilbert syndrome is a hereditary, relatively common, benign, unconjugated hyperbilirubinaemia (high bilirubin levels in the blood). Gilbert syndrome is generally considered to be an autosomal recessive disorder. However, there have been cases of heterozygosity and compound heterozygosity reported in patients with Gilbert syndrome, particularly among the Asian population.
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Page title:GILBERT'S SYNDROME
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Description:Gilbert's syndrome is a common condition which may cause mild jaundice. This article outlines its benign nature and how it is diagnosed...
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