A case report of spondyloepiphyseal dysplasia congenita.

نویسندگان

  • Y Gembun
  • Y Nakayama
  • Y Shirai
  • M Miyamoto
  • T Sawaizumi
  • S Kitamura
چکیده

Spondyloepiphyseal dysplasia congenita (SED) is a rare form of skeletal systemic disease, characterized by congenital dwarfism with a short trunk and epiphysial dysplasia in the long bones and vertebral bodies. Patients also frequently suffer from atlanto-axial instability due to os odontoideum. Compression of the spinal cord caused by atlanto-axial instability is a common, serious complication in SED patients, and causes severe spinal cord symptoms or occasionally sudden death. We present an SED patient who underwent a posterior fusion of the occiput to the cervical spine for severe spinal cord symptoms due to atlanto-axial instability.

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عنوان ژورنال:
  • Journal of Nippon Medical School = Nippon Ika Daigaku zasshi

دوره 68 2  شماره 

صفحات  -

تاریخ انتشار 2001