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A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I

BACKGROUND: Neurofibromatosis type 1 is an autosomal dominant genetic disease with characteristic café-au-lait spots, neurofibroma, and dystrophic changes in the bones. However, complications involving atlanto-axial dislocation are rare. CASE PRESENTATION: We report a case of neurofibromatosis with...

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Detalles Bibliográficos
Autores principales: Kinoshita, Hayato, Miyakoshi, Naohisa, Kobayashi, Takashi, Abe, Toshiki, Kikuchi, Kazuma, Shimada, Yoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485174/
https://www.ncbi.nlm.nih.gov/pubmed/31023294
http://dx.doi.org/10.1186/s12893-019-0502-z