Why is it called Gilbert syndrome? What is another name for Gilbert’s syndrome?

Gilbert’s syndrome is an inherited condition often discovered by accident, such as when someone has a blood test. It occurs due to a defect in the processing of bilirubin by the liver. The syndrome may cause the skin and the whites of the eyes to have a yellow tinge due to the build-up of bilirubin.
Gilbert’s syndrome is typically harmless and treatment isn’t required.

Why is it called Gilbert syndrome?

Gilbert syndrome was first described by French gastroenterologist Augustin Nicolas Gilbert and co-workers in 1901. In German literature, it is commonly associated with Jens Einar Meulengracht. Alternative, less common names for this disorder include Familial benign unconjugated hyperbilirubinemia.

What is another name for Gilbert’s syndrome?

Gilbert’s syndrome. Other names. Gilbert syndrome, Meulengracht syndrome, Gilbert-Lereboullet syndrome, hyperbilirubinemia Arias type, hyperbilirubinemia type 1, familial cholemia, familial nonhemolytic jaundice. Bilirubin.

Bilirubin is yellow liquid waste that occurs naturally as the body breaks down old red blood cells. People with Gilbert’s syndrome don’t produce enough liver enzymes to keep bilirubin at a normal level.