Gilbert’s Syndrome, UGT1A1: More Than Meets The Eye
Gilbert’s syndrome is a condition involving a genetic polymorphism in a phase 2 glucuronidation gene known as UGT1a1. The result of this causes elevations in the levels of unconjugated bilirubin. The current scientific consensus is that Gilbert’s is a relatively benign condition, that only features elevations of bilirubin. I strongly disagree with that contention. A