首页> 外文期刊>Case Reports in Orthopedics >The Treatment of Cleidocranial Dysostosis (Scheuthauer-Marie-Sainton Syndrome), a Rare Form of Skeletal Dysplasia, Accompanied by Spinal Deformities: A Review of the Literature and Two Case Reports
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The Treatment of Cleidocranial Dysostosis (Scheuthauer-Marie-Sainton Syndrome), a Rare Form of Skeletal Dysplasia, Accompanied by Spinal Deformities: A Review of the Literature and Two Case Reports

机译:颅骨发育不良(Scheuthauer-Marie-Sainton综合征),一种罕见的骨骼发育不良形式,伴有脊柱畸形的治疗:文献综述和两例病例报告

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Cleidocranial dysostosis is a skeletal dysplasia inherited in an autosomal dominant manner and may lead to complications such as scoliosis and kyphosis, concurrent with various orthopedic involvements. Since concurrent spinal deformities are of progressive nature, surgical treatment may be necessary. In addition to other orthopedic problems, possible accompanying complications such as atlanto-axial subluxation, myelopathy, syringomyelia, congenital spine deformities, spondylosis, and spondylolisthesis should be kept in mind while planning for the treatment of scoliosis and kyphosis. Lengthening the use of growth-friendly systems (growing rod) in patients, like ours, with an early onset of symptoms, and performing posterior instrumentation and fusion once the spinal growth is complete will yield successful results with no complications in the middle and the long term. Further multicenter studies with more comprehensive assessments are required to find solutions to spinal problems related to this rare skeletal dysplasia.
机译:颅骨发育不良是一种以常染色体显性遗传的遗传性骨骼发育不良,可能导致诸如脊柱侧凸和后凸畸形的并发症,并伴有各种骨科疾病。由于并发性脊柱畸形具有渐进性,因此可能需要手术治疗。除其他骨科问题外,在计划治疗脊柱侧凸和后凸畸形时,应牢记可能伴有的并发症,例如寰枢椎半脱位,脊髓病,脊髓空洞症,先天性脊柱畸形,脊椎病和脊椎滑脱。像我们这样的患者,在症状较早发作时延长对患者友好的生长系统(生长杆)的使用,并在脊柱生长完成后进行后路器械和融合术将获得成功的结果,而中长期无并发症术语。需要进一步的多中心研究和更全面的评估,以找到与这种罕见的骨骼发育不良相关的脊柱问题的解决方案。

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