{"id":11149,"date":"2025-07-27T09:27:42","date_gmt":"2025-07-27T07:27:42","guid":{"rendered":"https:\/\/valintermed.com\/?p=11149"},"modified":"2025-07-27T09:27:42","modified_gmt":"2025-07-27T07:27:42","slug":"essentsialnaya-pentozuriya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/essential-pentosuria\/","title":{"rendered":"Essential pentosuria"},"content":{"rendered":"
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Essential pentosuria (EP) is a rare hereditary disorder caused by a deficiency of an enzyme involved in the metabolism of pentoses, particularly ribose and arabinose. This condition is characterized by excessive excretion of pentoses into the urine, which can lead to various metabolic dysfunctions. The process caused by these disorders is often accompanied by clinical manifestations such as slight weight loss, fatigue, and changes in the quality of life of patients. In addition, this metabolic disorder is being studied by doctors, as its consequences can be much more serious than initially thought.<\/p>\n

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