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
16
A child with metabolic liver disease has hepatomegaly and recurrent hypoglycemia. Which diagnostic test confirms enzyme deficiency?
A
Ultrasound abdomen
B
Genetic testing
C
Chest X ray
D
Urine analysis

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