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Unknown General 77ed8ce5

McArdle's disease is due to deficiency of -

A
Branching enzyme
B
Glucose 6 phosphatase
C
Acid maltase deficiency
D
Muscle phosphorylase
High-Yield Explanation
Ans. is 'd' i.e., Muscle phosphorylase Type Enzyme deficiencyOrgan (s) affected1von Gierke's diseaseGlucose 6-phosphataseLiver, kidney11Pompe's diseasea (1 - 4) Glucosidase (acid maltase)All organsIIICori's disease/Forbe's diseaseDebranching enzymeMuscle, liverIVAndersen's diseaseBranching enzymeLiver, myocardiumVMcArdle's diseaseMuscle PhosphorylaseMuscleVIHers' diseasePhosphorylaseLiverVIITarui's diseasePhosphofructokinaseMuscle, RBCsVIII Phosphorylase kinaseLivero There is also on X-ltnked form of phosphorylase kinase deficiency. This is sole exception as all other glycogen storage diseases are inherited as autosomal recessive trait.

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