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OpenStudy (anonymous):
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? Avoidance of foods containing any type of carbohydrate Decreased intake of simple carbohydrates in the morning Frequent feedings of complex carbohydrates throughout the day Monitoring consumption of refined sugars and simple carbohydrates
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OpenStudy (aaronq):
Please put some thought into your question when you type it, don't simply copy and paste.
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