Exam: Liver Disorders in Children: Hereditary Hyperbilirubinemia, Crigler Najjar Syndrome, Gilbert Syndrome, Dubin Johnson Syndrome, Rotor Syndrome, Neonatal Cholestasis, Wilson Disease, Glycogen Storage Disease in Paediatrics
30:00
4
A 9-year-old child has chronic mild conjugated hyperbilirubinemia with normal liver enzymes. Liver biopsy is normal without pigmentation. Urinary coproporphyrin excretion is increased. What is the most likely diagnosis?