What is the primary enzyme deficiency responsible for the development of Pompe disease, a genetic disorder characterized by the accumulation of glycogen in muscles?

A Acid alpha-glucosidase
B Alpha-amylase
C Glucosidase II
D Debranching enzyme
Pompe disease is caused by a deficiency of acid alpha-glucosidase, an enzyme that breaks down glycogen in lysosomes.
National Institutes of Health (NIH)
Enzymes in Disease Genetic Disorders Lysosomal Storage Diseases Hard MEDICAL Confidence: high