Existence of gilbert's syndrome and hepatitis at the same time

Abstract

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