{"id":12973,"date":"2024-08-23T07:21:20","date_gmt":"2024-08-23T05:21:20","guid":{"rendered":"https:\/\/valintermed.com\/?p=12973"},"modified":"2024-08-23T07:21:20","modified_gmt":"2024-08-23T05:21:20","slug":"sindrom-sotosa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sotosa-syndrome\/","title":{"rendered":"Sotos syndrome"},"content":{"rendered":"
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Sotos syndrome is a rare genetic disorder that belongs to a group of syndromes associated with premature aging. Named after pediatrician K. B. Sotos, the disorder is characterized by a variety of clinical features, the most common of which are hypertrophy, prominent facial features, micrognathia, and varying degrees of cognitive impairment. Sotos syndrome is caused by abnormalities in the development and formation of tissues, which leads to a decrease in the functions of various organs and systems. Research shows that patients with this syndrome may have an increased predisposition to various diseases, including cardiovascular and metabolic disorders.<\/p>\n

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