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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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Autori principali: Zineb Izi, MD, Kaoutar Imrani, MD, Najwa Amsiguine, MD, Tlaite Oubaddi, MD, Nabil Moatassim Billah, PhD, Ittimade Nassar, PhD
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elsevier 2023-08-01
Serie:Radiology Case Reports
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Accesso online:http://www.sciencedirect.com/science/article/pii/S1930043323003114
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