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Background : Gilbert's syndrome is a chronic or recurrent mild unconjugated hyperbilirubinemia caused by decreased activity of UDP glucuronosyltranferase ( UGT1A1 ). The most common cause of Gilbert's syndrome in Caucasians is homozygous variant of the A(TA) 7 TAA promoter polymorphism. Alleles with five or eight TA repeats have also been described, but they are very rare in Caucasian populations.

Rare TA repeats in promoter TATA box of the UDP glucuronosyltranferase ( UGT1A1 ) gene in Croatian subjects