Which type of glycogen storage disease is characterized by a deficiency of lysosomal acid alpha-glucosidase?
A) type III
B) type IV
C) type V
D) type II
E) type VI

Question

Quizplus · Accepted Answer

Type II glycogen storage disease, also known as Pompe disease, is characterized by a deficiency of the lysosomal enzyme acid alpha-glucosidase. This leads to the accumulation of glycogen in lysosomes and can cause muscle weakness, respiratory problems, and heart disease.

Which Type of Glycogen Storage Disease Is Characterized by a Deficiency