Breitling Magnus, Lemire Edmond G, Rabin Michael
Department of Medical Imaging, University of Saskatchewan, Saskatoon, S7N 0W8, Saskatchewan, Canada.
Pediatr Radiol. 2006 Aug;36(8):866-9. doi: 10.1007/s00247-006-0181-7. Epub 2006 Jun 8.
Spondylocarpotarsal synostosis syndrome (SSS) is a rare autosomal recessive condition characterized primarily by vertebral malsegmentation, carpal/tarsal coalition, and a dysmorphic appearance. Differentiating SSS from other congenital scoliosis syndromes requires evaluation of the vertebrae, ribs, soft tissues, and spinal cord. The enhanced resolution over plain radiographs seen with MRI allows more detailed assessment of vertebral malformation and surrounding anatomy. Diagnosis of the underlying cause of congenital scoliosis might be enhanced using this technology. We report on a 12-year-old girl of unaffected parents with SSS who was evaluated with MRI sequences of the spine to show various types of malsegmentation. Additionally, there is the new finding of fusion of teeth, with developmental failure of a canine incisor.
脊椎腕跗骨联合综合征(SSS)是一种罕见的常染色体隐性疾病,主要特征为椎体节段异常、腕骨/跗骨联合以及畸形外观。将SSS与其他先天性脊柱侧凸综合征区分开来需要对椎体、肋骨、软组织和脊髓进行评估。MRI相对于平片具有更高的分辨率,能够更详细地评估椎体畸形及周围解剖结构。使用这项技术可能会提高对先天性脊柱侧凸潜在病因的诊断。我们报告了一名12岁患SSS的女孩,其父母未患病,对其进行了脊柱MRI序列检查,显示出各种类型的节段异常。此外,还发现了新的牙齿融合情况,一颗犬齿门牙发育不全。