{"id":13082,"date":"2024-08-23T05:31:48","date_gmt":"2024-08-23T03:31:48","guid":{"rendered":"https:\/\/valintermed.com\/?p=13082"},"modified":"2024-08-23T05:31:48","modified_gmt":"2024-08-23T03:31:48","slug":"spondiloepimetafizarnaya-displaziya-tipa-strudvika","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spondylotic-epithelial-displasia-of-the-strudvika-type\/","title":{"rendered":"Spondyloepimetaphyseal dysplasia Strudwick type"},"content":{"rendered":"
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Spondyloepimetaphyseal dysplasia of the Strudwick type (or Strudwick dysplasia) is a rare hereditary disease belonging to the group of connective tissue dysplasias, characterized by developmental anomalies of the spine and limbs. The main clinical manifestations are vertebral dysplasia, short limbs, deformities of the shoulder girdle and femurs, as well as various steirioses and joint dysfunctions. Given the multisystem nature of the disease, it can be accompanied by various neurological and orthopedic complications, requiring a multi-level approach to diagnosis and treatment.<\/p>\n

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