Answer:
Pompe's disease is also known as glycong type 2 disease. it is an autosomal recessive disease in which the lysosome is unable to metabolize glycogen due to the absence of acid aplha glucosidase enzyme. As a result glycogen are stored in liver and muscle cells.
if an infected liver with popme's disease is observed under electron micrograph, a large granules of glycogen will be seen.
