Congenital non-hemolytic jaundice
Congenital non-hemolytic jaundice (Gilbert Syndrome) is a comprehensive group of diseases. It was first reported by the French physician Gilbert in 1092, which is caused by non-hemolytic, non-binding bilirubinemia. 25% to 50% of congenital patients have this disease, which is an autosomal dominant genetic disease. Strictly defined, it is characterized by non-hemolytic, non-binding hyperbilirubinemia, normal serum bile acid, and normal liver function.
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