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    SubjectsPediatricsGenetic & Metabolic Disorders — Lysosomal Storage Diseases (Sphingolipidoses)
    ClinicalPediatrics

    Genetic & Metabolic Disorders — Lysosomal Storage Diseases (Sphingolipidoses)

    1 MCQs in Pediatrics for NEET PG

    1 Hard
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    Sample Questions

    hard

    A 2-year-old boy from a consanguineous family presents with progressive neurological deterioration, cherry-red spot on the macula, and hepatosplenomegaly. Enzyme assay reveals deficiency of hexosaminidase A and B. Which of the following metabolic pathways is primarily affected?

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