Congenital non-hemolytic jaundice
Congenital non-hemolytic jaundice (Gilbert syndrome) is a group of comprehensive diseases. It was first reported by French physician Gilbert in 1092. It is jaundice caused by non-hemolytic and non-conjugated hyperbilirubinemia. 25% to 50% of congenital patients have this disease in their families. It is an autosomal dominant genetic disease. From a strict definition, it is characterized by non-hemolytic and non-conjugated hyperbilirubinemia, normal serum bile acid and normal liver function.
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Site of disease:
Hepatobiliary -
Infectious :
Not contagious -
Frequent population:
All -
Related symptoms:
Bile excretion is blocked obstructive jaundice fatigue indigestion fatigue -
Concurrent disease: