Type I glycogen storage disease is an inherited disorder in which patients are able to store glycogen in the liver but lack a necessary enzyme to break down glycogen properly. Based on the function of glycogen in the body, what would be the treatment for this disorder?

The correct answer is -  Frequent feeding of complex carbohydrates throughout the day

Explanation:

In type I glycogen disease person is able to store the glycogen in the liver however, the person lacks enzyme glucose -6-phosphatase for breaking the glycogen into glucose which leads to a decrease in the sugar level.

So. the treatment must prevent this hypoglycemia condition by taking such carbohydrates that can easily be digested and broken down to glucose like a complex carbohydrate.

Thus, the correct answer is -  Frequent feeding of complex carbohydrates throughout the day

only about ten percent of the energy at one trophic level is passed on to organisms at the next trophic level. the remainder of the energy is used in life processes or lost as heat.