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Pediatrics Disorders of Amino acid Metabolism 265980c2

A 6-month-baby presented with recurrent seizures and developmental delay. On examination there was alopecia and scaly skin rashes. Investigations revealed metabolic acidosis, elevated lactates & ketonuria. What could be the underlying enzyme deficiency?

A
Phenylalanine hydroxylase
B
Epimerase
C
Multiple carboxylase
D
Glucose 6 phosphatase
High-Yield Explanation
Skin rashes with presence of ketones and metabolic acidosis are all features of Multiple carboxylase deficiency. Phenylalanine hydroxylase deficiency- microcephaly, hypopigmentation, musty body odour Glucose 6 phosphatase deficiency- doll like facies

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