Literature DB >> 16270692

Occipitocondylar hyperplasia: an unusual craniovertebral junction anomaly causing myelopathy. Case report.

Chima Ohaegbulam1, Eric J Woodard, Mark Proctor.   

Abstract

The authors of this brief case report describe a previously unreported developmental variant of the craniovertebral junction. A 10-year-old girl who presented with cervical myelopathy was found to have cervicomedullary compression by hypertrophic occipital condyles. Decompression was achieved via a midline dorsal approach with no complications. The embryology of this area is briefly reviewed to attempt to explain the origin of this anomaly.

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Year:  2005        PMID: 16270692     DOI: 10.3171/ped.2005.103.4.0379

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  2 in total

1.  Bilateral occipito-condylar hyperplasia: a very rare anomaly treated with endoscopic endo-nasal approach.

Authors:  Keyvan Tayebi Meybodi; Farzad Tajik; Seyed Mousa Sadrhosseini; Farideh Nejat; Mehdi Zeinalizadeh
Journal:  Childs Nerv Syst       Date:  2015-05-06       Impact factor: 1.475

2.  Spontaneously improving occipitocondylar hyperplasia: a case report.

Authors:  Laszlo Nagy; Coby Ray
Journal:  J Neurol Surg Rep       Date:  2014-05-28
  2 in total

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