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Multifocal Head and Neck Neurofibromas with Osseous Abnormalities and Muscular Hypoplasia in a Child with Neurofibromatosis: Type I
Neurofibromatosis type 1 (NF1) is a clinically and genetically distinct disease involving both neuroectodermal and mesenchymal derivatives. Orofacial manifestations in NF1 have been documented before but occurrence of multifocal intraosseous (IO) and extraosseous (EO) neurofibromas is rare. The pres...
Autores principales: | Rath, Rachna, Kaur, Sheetal, Baig, Shadab Ali, Pati, Punyashlok, Sahoo, Sonalisa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921149/ https://www.ncbi.nlm.nih.gov/pubmed/27382495 http://dx.doi.org/10.1155/2016/3980270 |
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