Pediatric familial non-hemolytic jaundice syndrome

Familial non-hemolytic jaundice syndrome (Gilbert syndrome) is a group of comprehensive symptoms with jaundice as the main clinical manifestations, and is often a hereditary genetic disease. Because 25% of patients' parents and 50% of siblings show elevated serum bilirubin, some scholars believe that the symptoms may be transmitted by dominant genes with incomplete penetrance. The symptoms are also known as Gilbert syndrome, Gilbert disease, hyperbilirubinemia type I, congenital non-hemolytic jaundice-non-combined type, Gilbert-Lereboullet syndrome, Meulengracht syndrome, constitutional liver dysfunction syndrome, adolescents Intermittent jaundice, physiological hyperbilirubinemia, etc.