{"id":12097,"date":"2025-03-13T22:19:02","date_gmt":"2025-03-13T21:19:02","guid":{"rendered":"https:\/\/valintermed.com\/?p=12097"},"modified":"2025-03-13T22:19:02","modified_gmt":"2025-03-13T21:19:02","slug":"mnozhestvennyy-defitsit-karboksilazy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/multiple-karboksilazy-deficit\/","title":{"rendered":"Multiple carboxylase deficiency"},"content":{"rendered":"
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Multiple carboxylase deficiency is a rare genetic disorder characterized by insufficient activity of carboxylases, key enzymes in carbohydrate and fat metabolism. These enzymes play an important role in the biosynthesis of essential metabolites and the regulation of glycolysis, making them essential for normal cellular function. Deficiency of carboxylases can lead to a variety of metabolic disorders, problems at the level of biochemical processes, which ultimately affect the patient's general condition and can be life-threatening. Symptoms of the disease can range from mild to severe and may include growth retardation, delayed psychomotor development, and a variety of cardiac and neurological symptoms.<\/p>\n

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