Literature DB >> 11301365

A case report of spondyloepiphyseal dysplasia congenita.

Y Gembun1, Y Nakayama, Y Shirai, M Miyamoto, T Sawaizumi, S Kitamura.   

Abstract

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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Year:  2001        PMID: 11301365     DOI: 10.1272/jnms.68.186

Source DB:  PubMed          Journal:  J Nippon Med Sch        ISSN: 1345-4676            Impact factor:   0.920


  3 in total

1.  Atlantoaxial dislocation in a patient with nonsyndromic symmetrical dwarfism: Report of a rare case.

Authors:  Duvuru Ram; Venkatesh S Madhugiri; V R Roopesh Kumar; Reena Gulati; Gopalakrishnan M Sasidharan; Sudheer Kumar Gundamaneni
Journal:  J Craniovertebr Junction Spine       Date:  2015 Jan-Mar

2.  Management of Craniocervical Instability in Spondyloepiphyseal Dysplasia Congenita: Assessment of Literature and Presentation of Two Cases.

Authors:  Cody J Falls; Paul S Page; Garret P Greeneway; James A Stadler
Journal:  Cureus       Date:  2022-07-19

3.  Osteoarthritis in a fifty-year-old patient with unfused skeleton due to undiagnosed coexisting cleidocranial and spondyloepiphyseal dysplasia - Case report.

Authors:  Dr Mahum Zaidi; Sareema Eman Akhtar; Saad Shakil; Dr Muhammad Wasif; Dr Rabiya Siraj; Talal Almas; Joshua Ramjohn; Maha Alkhattab; Reema Ahmed; Tushar Thakur
Journal:  Ann Med Surg (Lond)       Date:  2022-06-28
  3 in total

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