Gilbert Syndrome is a genetic liver disease with low levels of the enzymes that handle bilirubin. Bilirubin is made when blood cells break down.
Gilbert Syndrome is more common in men than women and shows up in the teen years.
United States: 3-7% of people
Worldwide: 2-10% of Caucasians, 2% of Japanese and Eastern Asians, 20% of Indian, Southern Asian and Middle Eastern peoples
Excellent. Gilbert’s Syndrome does not change the liver’s health or change a patient’s lifespan.
Mildly increased levels of one type of bilirubin in the blood. This is called hyperbilirubinemia.
Most people have no symptoms. Sometimes when the body is stressed, the bilirubin gets even higher. This can lead to yellow skin and eyes (jaundice). Body stress can happen with illness, menstruation, dehydration, fasting (skipping meals), too much exercise and with certain medications.
To make the diagnosis and to rule out other liver diseases when bilirubin levels are high.
Low amounts of the liver enzymes that break down bilirubin.
Family history because this is a genetic condition.
Patients with high levels of bilirubin.
Blood tests that show high bilirubin without other causes of liver disease. A liver biopsy is rarely needed. If done it shows normal cells. Unnecessary testing should not be done.
Observation. Because there are no symptoms or damage to the liver there is no other treatment needed.
Yes- including pigmented gallstones, jaundice as a newborn. There is a risk of having toxic drug levels when taking medications that alter bilirubin break down. Some of those medications include: atazanavir, indinavir, acetaminophen, tyrosine kinase inhibitors, nonsteroidal anti-inflammatory drugs, statins, ezetimibe, oxazepam, lorazepam, lamotrigine, cyclosporin A, rifampin, ethinylestradiol, buprenorphine, menthol, and tocilizumab.
Victoria Howard, PA, University of Rochester, Rochester, NY – Updated December 2025.