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Glycogen storage disease type VI is a type of glycogen storage disease caused by a deficiency in liver glycogen phosphorylase.
It is also known as “Hers’ disease”, after Henri G. Hers, who characterized it in 1959.[1][2]
Patients generally have a benign course, and typically present with hepatomegaly[3] and growth retardation early in childhood. Mild hypoglycemia, hyperlipidemia, and hyperketosis may occur. Lactic acid and uric acid levels are normal.
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