{"id":11157,"date":"2025-07-27T08:58:33","date_gmt":"2025-07-27T06:58:33","guid":{"rendered":"https:\/\/valintermed.com\/?p=11157"},"modified":"2025-07-27T08:58:33","modified_gmt":"2025-07-27T06:58:33","slug":"anemiya-fankoni","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/anemia-fankoni\/","title":{"rendered":"Fanconi anemia"},"content":{"rendered":"
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Fanconi anemia is a rare hereditary disorder characterized by renal dysfunction and multiple systemic manifestations. This pathology belongs to a group of hereditary diseases associated with impaired reabsorption in the proximal tubules of the kidneys, which leads to the loss of important substances such as glucose, amino acids, bicarbonate and phosphates. One of the main clinical manifestations of Fanconi anemia is metabolic recurrent acidosis, as well as the development of osteomalacia and secondary hyperparathyroidism. The disease also often leads to the formation of kidney stones, phosphate-resistant osteopenia and problems with growth and development in children.<\/p>\n

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