Gilbert's syndrome
Gilbert's Syndrome is an inherited condition, first described in 1901 by French gastroenterologist Augustin Nicolas Gilbert and found in approx 5 - 10% of the population. It is the most common hereditary cause of increased levels of bilirubin, a yellowish pigment normally found in small amounts in blood and urine.
Gilbert's Syndrome is caused by changes in the DNA sequence of the gene that produces an enzyme that helps the body clear bilirubin from the body.
Symptoms
The main symptom of this otherwise harmless condition is a mild jaundice (yellowing) of the skin and eyes which is usually mild and requires no treatment. Certain activities (such as missing meals, lack of sleep, vigorous exercise, illness and stress) may make these symptoms worse by placing further stress upon the liver.
| Medicare Rebate available: | No, this test is not covered by Medicare |
| Specimen Type required: | Blood |
| Results available from your Doctor: | 5-7 days |