Common "Gilbert's Syndrome" queries answered by top doctors | iCliniq

Gilbert's Syndrome

"Gilbert's syndrome is a genetic liver disorder in which the liver cannot properly process bilirubin. People with this syndrome do not produce enough liver enzymes to keep bilirubin levels normal, leading to excess bilirubin building up in the body (hyperbilirubinemia). As a result, Gilbert's syndrome may present with dark-colored urine or clay-colored stool, dizziness, diarrhea, nausea, flu-like symptoms, and loss of appetite. Gilbert's syndrome does not require any treatment. The high bilirubin levels in the blood may fluctuate over time and lead to jaundice occasionally, which usually resolves on its own with no side effects.

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I have abnormal bilirubin levels but no symptoms. Why?

Query: Hi doctor, I am a 26 year old male, and I am a triathlete. Seven years back, I suffered from jaundice. I check my blood bilirubin every six months and liver function test every year. The result showed abnormal bilirubin level; the total bilirubin was 3.5. The LFT was normal. I also got an ultrasound...  Read Full »


Dr. Rosita Alizadeh Shalchi

Answer: Hello, Welcome to icliniq.com. I can imagine that you are concerned about your liver. I understand that you do not have any discomfort and ultrasound is normal. Your test result is compatible with a harmless condition named Gilbert's syndrome. In this syndrome, a pigment named bilirubin is no...  Read Full »

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