Gilbert's Syndrome

Gilbert’s syndrome also called zheel-BAYR syndrome, is the most common hereditary cause of increased bilirubin. Due to genetic failure to make the enzyme UGT1A1 that breaks down the bilirubin enzyme hyperbilirubinemia occurs. GS is found in up to 5% of the population. Experteam offers a complete system for genetic analysis of Gilbert’s syndrome.

Download PDF

Gilbert's Syndrome
Ref.ProductTechnology SizeRegulatoryAdditional Info
GS.01FLGilbert Syndrome Kit-FL

Capillary Electrophoresis Kit


Appl. Bios. & Beckman Coult.