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Solitary Epicranial Neurofibroma with Neurofibromatosis Type 1-Related Germline Mutation: Case Report
A 33-year-old male became aware of a painless soft mass in the left occipital region. His medical and family history were unremarkable for neurofibromatosis type 1 (NF1) or other genetic disorders. Physical examination showed no signs of NF1. Neurological and ophthalmological examinations found no a...
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| Publicado no: | Neurol Med Chir (Tokyo) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Japan Neurosurgical Society
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4533480/ https://ncbi.nlm.nih.gov/pubmed/24140765 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2176/nmc.cr2012-0364 |
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