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When functioning properly, the liver: breaks down fats using bile stored in the gall bladder. In a person with Gilbert’s syndrome, the liver is unable to consistently process the yellowish–brown pigment in bile, called bilirubin. This leads to high levels of bilirubin in the bloodstream, which can cause the skin and eyes to turn yellow (jaundice).

Despite the person’s jaundiced appearance, the functioning of their liver is normal. Gilbert’s syndrome is a common, mild disorder thought to be inherited in around half of all cases. Men are at higher risk than women and tend to develop Gilbert’s syndrome between their late teens and early 30s.

Usually, the disorder is diagnosed by chance during the investigation of unrelated illnesses. Gilbert’s syndrome is considered a harmless condition and typically does not need treatment. Gilbert’s syndrome typically has no obvious symptoms, other than yellowing of the skin or eyes (jaundice).

Other symptoms are sometimes reported, including: abdominal pain

However, it is not clear that these symptoms are directly related to higher levels of bilirubin.

A person with Gilbert’s syndrome has normal (straw-coloured) urine.

A person with hepatitis will usually have dark urine and may also have a fever. Bilirubin is the yellowish-brown pigment that gives bile its colour. It is created by the breakdown of old red blood cells by the spleen.

Further processing of bilirubin happens within the liver

Gilbert’s syndrome occurs due to the reduced activity of a liver enzyme that makes the liver less capable of processing bilirubin. This leads to greater than normal levels of bilirubin circulating in the bloodstream, which can cause yellowing of the skin and eyes. In a person with Gilbert’s syndrome, the bilirubin levels typically fluctuate and only sometimes hover within the normal range.

In many cases, Gilbert’s syndrome is so mild that there are no obvious symptoms. It is often diagnosed by accident when blood tests are ordered to investigate an unrelated condition. In other cases, Gilbert’s syndrome may be accompanied by symptoms similar to more serious liver diseases, so thorough medical investigation is needed.

Diagnostic tests include:

  • urine tests. A genetic test exists that can detect the gene that causes Gilbert’s syndrome
  • but this is not usually necessary for a diagnosis
  • is not widely available. Gilbert’s syndrome is a mild disorder that typically doesn’t need medical treatment

People with the disorder lead normal, healthy lives. There is no evidence to suggest that the condition is harmful or leads to more serious diseases. Occasionally, the presence of Gilbert’s syndrome may increase the toxicity of certain drugs used for therapy of severe disorders.

These drugs include irinotecan (used in the treatment of cancer) and indinavir (used in the treatment of HIV/AIDS). There is no evidence that Gilbert’s syndrome has any effect on most commonly used medicines.

However, a patient with Gilbert’s syndrome would be wise to seek further advice from their medical practitioner before starting a new medication.

About Gilbert’s syndrome filters impurities and toxins from the body processes proteins and carbohydrates Symptoms of Gilbert’s syndrome gastrointestinal complaints fatigue weakness Processing bilirubin Diagnosing Gilbert’s Syndrome medical history physical examination blood tests Treatment is not necessary Certain medications may be affected Where to get help Your (GP) doctor Gastroenterologist Gilbert’s syndrome , Helen DeVos Children’s Hospital, Grand Rapids.

Key Points

  • This leads to high levels of bilirubin in the bloodstream, which can cause the skin and eyes to turn yellow (jaundice)
  • Gilbert’s syndrome is a common, mild disorder thought to be inherited in around half of all cases
  • Men are at higher risk than women and tend to develop Gilbert’s syndrome between their late teens and early 30s
  • Gilbert’s syndrome is considered a harmless condition and typically does not need treatment
  • Gilbert’s syndrome typically has no obvious symptoms, other than yellowing of the skin or eyes (jaundice)