{"id":13002,"date":"2024-08-23T06:51:26","date_gmt":"2024-08-23T04:51:26","guid":{"rendered":"https:\/\/valintermed.com\/?p=13002"},"modified":"2024-08-23T06:51:26","modified_gmt":"2024-08-23T04:51:26","slug":"sindrom-spondilokarpotarzalnogo-sinostoza","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spondylotic-carpotarzal-sinusitis-syndrome\/","title":{"rendered":"Spondylocarpotarsal synostosis syndrome"},"content":{"rendered":"
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Spondylocarpotarsal synostosis syndrome (SCTS) is a rare hereditary disease characterized by developmental abnormalities of the spine, upper and lower extremities. Changes occur at the level of short fingers and toes, as well as in the area of joint connections, which leads to intracranial dysplasia, dysfunction of the musculoskeletal system and the occurrence of various concomitant diseases. SCTS belongs to the group of congenital disorders, there are still many questions about its etiology and pathogenesis. Symptoms vary from mild anatomical abnormalities to significant functional disorders that seriously affect the quality of life of patients. The disease will require a comprehensive approach to diagnosis and treatment in order to minimize the consequences associated with difficulty in movement and improve the overall functional capabilities of patients.<\/p>\n

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