Coexistence of Gilbert syndrome with hereditary haemolytic anaemias
Journal of Clinical Pathology, 05/07/2012
Rawa K et al. – Genotyping of the UGT1A1 gene showed distinct distribution of the common A(TA)nTAA polymorphism relative to other European populations. Because of a greater risk of hyperbilirubinaemia due to hereditary haemolytic anaemia, the diagnosis of Gilbert syndrome in this group of patients is very important.