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A fortuitous discovery of a neurofibroma in a female patient with type 1 neurofibromatosis: a case report
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of inheritance. This congenital disease is characterized by a wide spectrum of clinical manifestations and degree of severity. This case report describes a female patient in her early 20s who presented wi...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SAGE Publications
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751173/ https://www.ncbi.nlm.nih.gov/pubmed/36510447 http://dx.doi.org/10.1177/03000605221139716 |