{"id":11318,"date":"2025-07-27T00:58:14","date_gmt":"2025-07-26T22:58:14","guid":{"rendered":"https:\/\/valintermed.com\/?p=11318"},"modified":"2025-07-27T00:58:14","modified_gmt":"2025-07-26T22:58:14","slug":"bolezn-nakopleniya-glikogena-tip-6","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/glycogen-storage-disease-type-6\/","title":{"rendered":"Glycogen storage disease type 6"},"content":{"rendered":"
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Glycogen storage disease type 6, also known as Eppler's disease or glycogenosis type 6, is a rare inherited disorder of carbohydrate metabolism. The disorder is characterized by a deficiency of the enzyme glycogen phosphorylase, which results in a disruption of the normal breakdown of glycogen in the liver. This results in excess accumulation of glycogen, which causes a variety of clinical manifestations. The disorder most often manifests itself in childhood and adolescence, with symptoms ranging from mild to severe and including hypoglycemia, an enlarged liver, and muscle weakness, among other manifestations.<\/p>\n

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