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
13
A 6-week-old infant with neonatal cholestasis has markedly elevated gamma glutamyl transferase (GGT). Which condition is most likely?
A
Biliary atresia
B
Progressive familial intrahepatic cholestasis
C
Gilbert syndrome
D
Crigler Najjar syndrome

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