{"id":11230,"date":"2025-07-27T05:26:07","date_gmt":"2025-07-27T03:26:07","guid":{"rendered":"https:\/\/valintermed.com\/?p=11230"},"modified":"2025-07-27T05:26:07","modified_gmt":"2025-07-27T03:26:07","slug":"semeynyy-dobrokachestvennyy-defitsit-medi","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/family-good-quality-deficit\/","title":{"rendered":"Familial benign copper deficiency"},"content":{"rendered":"
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Familial benign copper deficiency, also known as cystic copper fibrosis or Wilson's disease, is a genetic disorder associated with impaired copper metabolism in the body. This condition causes copper to accumulate in tissues, which can lead to damage to the liver, brain and other organs. The key aspect is the fact that copper deficiency in this context does not mean a lack of this micronutrient, but, on the contrary, its excess, which accumulates due to a disruption in normal metabolism. The disease can have a variety of clinical manifestations, including symptoms related to the nervous system, liver and other organ systems, and requires a comprehensive approach to diagnosis and therapy.<\/p>\n

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