Any of numerous types of hereditary enzyme deficiency resulting in altered metabolism of glycogen. The problems are classified in two groups, those affecting the liver and those involving striated muscle, both primary glycogen storage sites. Symptoms in the liver group range from symptomatic hypoglycemia with ketosis to asymptomatic liver enlargement (hepatomegaly). In the muscle group, they range from weakness and cramps to fatal heart enlargement.
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Principal storage carbohydrate of animals, occurring primarily in the liver and resting muscles. It is also found in various bacteria, fungi, and yeasts. Glycogen is a branched polysaccharide, a long chain of glucose units, into which it is broken down when energy is needed.
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