{"id":11255,"date":"2025-07-27T04:23:24","date_gmt":"2025-07-27T02:23:24","guid":{"rendered":"https:\/\/valintermed.com\/?p=11255"},"modified":"2025-07-27T04:23:24","modified_gmt":"2025-07-27T02:23:24","slug":"sindrom-freyzera","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/freaker-s-syndrome\/","title":{"rendered":"Fraser syndrome"},"content":{"rendered":"
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Fraser syndrome is a rare genetic disorder characterized by multiple developmental abnormalities, including malformations of the kidneys, genitals, and facial structures. The disorder is associated with a defect in the embryonic development of the body, which leads to a variety of abnormalities. The main clinical manifestations of the syndrome vary in severity and include various combinations of features such as cryptorchidism, abnormal formation of the external genitalia, and abnormal development of the kidneys and other organs. Fraser syndrome is often associated with a deterioration in quality of life, an increased risk of complications, and the need for multi-stage monitoring by physicians of different specialties.<\/p>\n

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