{"id":11680,"date":"2025-07-26T06:56:21","date_gmt":"2025-07-26T04:56:21","guid":{"rendered":"https:\/\/valintermed.com\/?p=11680"},"modified":"2025-07-26T06:56:21","modified_gmt":"2025-07-26T04:56:21","slug":"vrozhdennaya-pochechnaya-aminoatsiduriya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/congenital-renal-aminoaciduria\/","title":{"rendered":"Congenital renal aminoaciduria"},"content":{"rendered":"
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Congenital renal aminoaciduria is a genetic disorder characterized by impaired reabsorption of certain amino acids in the kidneys. This defect results in excessive excretion of amino acids in the urine, which can cause a variety of clinical symptoms and long-term consequences, depending on the type of amino acids involved in the pathological process. The disease is often associated with dysfunction of the proximal tubules of the kidneys, which can also lead to difficulties in protein metabolism and fluid and electrolyte imbalance. Treatment of this condition requires a comprehensive approach, including both drug therapy and dietary restrictions.<\/p>\n

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