Gilbert's Syndrome is a relatively common, harmless genetic condition that affects the functioning of the liver. It occurs when the liver is unable to process bilirubin properly, which results in an excess of bilirubin in the bloodstream.
Symptoms of Gilbert's Syndrome may include yellowing of the skin and eyes, fatigue, abdominal pain, and occasional mild jaundice. However, many people with Gilbert's Syndrome have no symptoms at all.
Gilbert's Syndrome is usually diagnosed through a blood test that measures the levels of bilirubin in the bloodstream. There is no specific treatment for the condition, but symptoms can be managed through various lifestyle changes and medications.
Most people with Gilbert's Syndrome can lead normal, healthy lives and are able to participate in regular activities with no issues. However, in rare cases, complications such as liver damage or anemia can occur.
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