Low-Grade Gliomas in Patients with Noonan Syndrome: Case-Based Review of the Literature

Noonan syndrome (NS) is a congenital autosomic dominant condition characterized by a variable spectrum from a clinical and genetical point of view. Germline mutations in more than ten genes involved in RAS–MAPK signal pathway have been demonstrated to cause the disease. An higher risk for leukemia a...

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Detalles Bibliográficos
Autores principales: Lodi, Mariachiara, Boccuto, Luigi, Carai, Andrea, Cacchione, Antonella, Miele, Evelina, Colafati, Giovanna Stefania, Diomedi Camassei, Francesca, De Palma, Luca, De Benedictis, Alessandro, Ferretti, Elisabetta, Catanzaro, Giuseppina, Pò, Agnese, De Luca, Alessandro, Rinelli, Martina, Lepri, Francesca Romana, Agolini, Emanuele, Tartaglia, Marco, Locatelli, Franco, Mastronuzzi, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460327/
https://www.ncbi.nlm.nih.gov/pubmed/32806529
http://dx.doi.org/10.3390/diagnostics10080582

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