Through rigorous, intermittent exercising and in the course of prolonged Bodily activity, muscle mass glycogen particles are damaged down, releasing glucose molecules that muscle cells then oxidize by means of anaerobic and aerobic processes to generate the adenosine triphosphate (ATP) molecules demanded for muscle contraction.1 The rate at which m

There are 2 most important types of glycogen storage illnesses: These ensuing from faulty glycogen homeostasis from the liver and those ensuing from defective glycogen homeostasis within the muscle. Diseases ensuing from defective liver glycogen storage typically bring about hepatomegaly (enlarged liver), hypoglycemia, and cirrhosis (liver scarring