Gilbert`s syndrome (constitutional hepatic disfunction, familial nonhemolitic jaundice and idiopatic unconjugated hyperbilirubinemia) is inherited as an autosomal recessive trait, characterized by the liver disorders and the absence of the indicators of hemolysis, rare clinic syndrome which appears with unconjugated bilirubinemia. The cause of this disease is mutation of uridine-di-phosphate glucuronosyltransferase
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