{"id":11314,"date":"2025-07-27T01:28:29","date_gmt":"2025-07-26T23:28:29","guid":{"rendered":"https:\/\/valintermed.com\/?p=11314"},"modified":"2025-07-27T01:28:29","modified_gmt":"2025-07-26T23:28:29","slug":"bolezn-nakopleniya-glikogena-5-go-tipa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/glycogen-storage-disease-type-5\/","title":{"rendered":"Glycogen storage disease type 5"},"content":{"rendered":"
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Glycogen storage disease type 5 (Glycogenosis 5) is a rare inherited metabolic disorder associated with the accumulation of glycogen that cannot be properly metabolized. The disease affects the muscles and liver, which in turn leads to various clinical manifestations, including muscle weakness and pain, and possible liver problems. The main cause of the disease is genetic mutations that affect the enzymes involved in glycogenolysis. The pathology manifests itself mainly in childhood or adolescence, although symptoms may appear in later life.<\/p>\n

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