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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Detalles Bibliográficos
Autores principales: SUGIYAMA, Natsuki, TSUTSUMI, Satoshi, AKIBA, Chihiro, NAKANISHI, Hajime, OGINO, Ikuko, YASUMOTO, Yukimasa, ARAI, Hajime, ITO, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533480/
https://www.ncbi.nlm.nih.gov/pubmed/24140765
http://dx.doi.org/10.2176/nmc.cr2012-0364

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533480/
https://www.ncbi.nlm.nih.gov/pubmed/24140765
http://dx.doi.org/10.2176/nmc.cr2012-0364

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