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...

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Detalles Bibliográficos
Autores principales: Rath, Rachna, Kaur, Sheetal, Baig, Shadab Ali, Pati, Punyashlok, Sahoo, Sonalisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
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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