Central nervous system manifestations of neurofibromatosis type 2: A case report

Neurofibromatosis type 2 (phacomatosis) is a rare inherited autosomal dominant condition defined by the development of numerous central neuronal tumors. In addition to classic intracranial schwannomas, intracranial and spinal meningiomas, and intramedullary ependymomas, it can be associated with a f...

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Detalles Bibliográficos
Autores principales: Izi, Zineb, Imrani, Kaoutar, Amsiguine, Najwa, Oubaddi, Tlaite, Billah, Nabil Moatassim, Nassar, Ittimade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300456/
https://www.ncbi.nlm.nih.gov/pubmed/37388263
http://dx.doi.org/10.1016/j.radcr.2023.05.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300456/
https://www.ncbi.nlm.nih.gov/pubmed/37388263
http://dx.doi.org/10.1016/j.radcr.2023.05.011

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