{"id":11247,"date":"2025-07-27T04:26:49","date_gmt":"2025-07-27T02:26:49","guid":{"rendered":"https:\/\/valintermed.com\/?p=11247"},"modified":"2025-07-27T04:26:49","modified_gmt":"2025-07-27T02:26:49","slug":"sindrom-fayngolda","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/fayngold-syndrome\/","title":{"rendered":"Feingold syndrome"},"content":{"rendered":"
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Feingold syndrome (or Feingold-Mendel syndrome, depending on the author's preference) is a rare genetic disorder belonging to the class of dysplastic syndromes. This syndrome is characterized by multiple abnormalities affecting tissues, organs, and systems of the body, such as developmental disorders, facial and dental abnormalities, and cognitive abnormalities. The most obvious clinical manifestations include abnormalities of the auricle, facial structures, and various dental disorders. The underlying cause of the syndrome is associated with mutations in individual genes associated with embryonic development and its development at the tissue level.<\/p>\n

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