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...

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Detalles Bibliográficos
Autores principales: Harrabi, Fathia, Methnani, Jabeur, Houssem, Ammar, Abdelkader, Mizouni, Mehdi, Ben Latifa, Amine, Saiid Mohamed, Mohamed, Ben Mabrouk, Ali, Ben Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Reports
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751173/
https://www.ncbi.nlm.nih.gov/pubmed/36510447
http://dx.doi.org/10.1177/03000605221139716

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