Orthopaedic manifestations of neurofibromatosis type 1: A case report

Neurofibromatosis type 1 (NF1) or von Recklinghausen disease is one of the most common autosomal dominant genetic diseases. It is characterized by ‘café-au-lait’ spots and multiple tumors starting from the central and peripheric nervous system. The diagnosis is determined on two out of seven criteri...

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Detalles Bibliográficos
Autores principales: Năstase, Florentina, Radaschin, Diana Sabina, Niculeț, Elena, Brădeanu, Andrei Vlad, Verenca, Mădălina Codruța, Nechita, Aurel, Chioncel, Valentin, Nwabudike, Lawrence Chukwudi, Baroiu, Liliana, Drima Polea, Eduard, Fotea, Silvia, Anghel, Lucretia, Nechifor, Alexandru, Tatu, Alin Laurenţiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756425/
https://www.ncbi.nlm.nih.gov/pubmed/35069816
http://dx.doi.org/10.3892/etm.2021.11058

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756425/
https://www.ncbi.nlm.nih.gov/pubmed/35069816
http://dx.doi.org/10.3892/etm.2021.11058

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