Low-Grade Gliomas in Patients with Noonan Syndrome: Case-Based Review of the Literature
Low-Grade Gliomas in Patients with Noonan Syndrome: Case-Based Review of the Literature
About this item
Full title
Author / Creator
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 and Mastronuzzi, Angela
Publisher
Basel: MDPI AG
Journal title
Language
English
Formats
Publication information
Publisher
Basel: MDPI AG
Subjects
More information
Scope and Contents
Contents
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 and solid malignancies, including brain tumors, is...
Alternative Titles
Full title
Low-Grade Gliomas in Patients with Noonan Syndrome: Case-Based Review of the Literature
Authors, Artists and Contributors
Author / Creator
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
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_2024a8889ec04032ae9f11e02e41b239
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2024a8889ec04032ae9f11e02e41b239
Other Identifiers
ISSN
2075-4418
E-ISSN
2075-4418
DOI
10.3390/diagnostics10080582
