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Multiple primary cranio-spinal tumours in a 13-year-old female with neurofibromatosis type 2 management strategy
INTRODUCTION: Neurofibromatosis type 2 (NF2) is an inherited, rare autosomal dominant syndrome characterised by the development of multiple benign cranial and spinal tumours, peripheral neuropathy, ophthalmological and cutaneous lesions. Herein, we report one case of NF2 treated with multivariate ch...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3015198/ https://ncbi.nlm.nih.gov/pubmed/20661577 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00381-010-1238-3 |
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