Gilbert’s disease is a common disorder passed down through families. It affects the way bilirubin is processed by the liver, and causes the skin to take on a yellow color (
Icterus intermittens juvenilis; Low-grade chronic hyperbilirubinemia; Familial non-hemolytic-non-obstructive jaundice; Constitutional liver dysfunction; Unconjugated benign bilirubinemia
Gilbert’s disease affects up 1 in 10 people in some Caucasian groups.
- Yellowing of the skin and whites of the eyes (mild jaundice)
In people with Gilbert’s syndrome, jaundice most often appears during times of exertion, stress, and infection, or when they do not eat.
Exams and Tests
A blood test for bilirubin shows changes that occur with Gilbert’s disease. The total bilirubin level is mildly elevated, with most being unconjugated bilirubin. Usually the total level is less than 2 mg/dL, and the conjugated bilirubin level is normal.
Gilbert’s disease is linked to a genetic problem, but genetic testing is not needed.
No treatment is necessary for Gilbert’s disease.
Jaundice may come and go throughout life. It is more likely to appear during illnesses such as colds. It does not cause health problems, but it can confuse the results of tests for jaundice.
There are no known complications.
When to Contact a Medical Professional
Call your health care provider if you have jaundice or pain in the abdomen that does not go away.
There is no proven prevention.