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
9
A child presents with hepatomegaly, severe fasting hypoglycemia, lactic acidosis, and hyperlipidemia. Enzyme analysis shows deficiency of glucose-6-phosphatase. What is the diagnosis?
A
Glycogen storage disease type I
B
Glycogen storage disease type II
C
Wilson disease
D
Tyrosinemia

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