{"id":13190,"date":"2024-08-23T03:45:02","date_gmt":"2024-08-23T01:45:02","guid":{"rendered":"https:\/\/valintermed.com\/?p=13190"},"modified":"2024-08-23T03:45:02","modified_gmt":"2024-08-23T01:45:02","slug":"sindrom-toriello-keri","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/toriello-keri-syndrome\/","title":{"rendered":"Toriello-Carey syndrome"},"content":{"rendered":"
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Toriello-Carey syndrome (TC) is a rare genetic disorder that belongs to the categories of autosomal dominant disorders associated with growth anomalies and development of various organs and systems. This disease is characterized by multiple facial anomalies, vascular pathology, short stature, and various neurological disorders. The syndrome was first described in clinical practice as a complex of symptoms arising due to genetic anomalies, which places it in a series of syndromes that require detailed study and understanding of their pathogenesis. The disease can have a variety of manifestations, which makes its diagnosis quite complex, and its treatment a multi-level process requiring a multidisciplinary approach.<\/p>\n

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