Cargando…
NF1-like optic pathway gliomas in children: clinical and molecular characterization of this specific presentation
BACKGROUND: Pediatric neurofibromatosis type 1 (NF1)–associated optic pathway gliomas (OPGs) exhibit different clinico-radiological features, treatment, and outcome compared with sporadic OPGs. While NF1-associated OPGs are caused by complete loss-of-function of the NF1 gene, other genetic alteratio...
Autores principales: | Lobón-Iglesias, María Jesús, Laurendeau, Ingrid, Guerrini-Rousseau, Léa, Tauziède-Espariat, Arnault, Briand-Suleau, Audrey, Varlet, Pascale, Vidaud, Dominique, Vidaud, Michel, Brugieres, Laurence, Grill, Jacques, Pasmant, Eric |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317061/ https://www.ncbi.nlm.nih.gov/pubmed/32642735 http://dx.doi.org/10.1093/noajnl/vdz054 |
Ejemplares similares
-
Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities
por: Gilbert-Dussardier, Brigitte, et al.
Publicado: (2016) -
One NF1 Mutation may Conceal Another
por: Pacot, Laurence, et al.
Publicado: (2019) -
HGG-40. NF1 mosaicism in a CMMRD-patient with a glioblastoma
por: Guerrini-Rousseau, Lea, et al.
Publicado: (2022) -
Pediatric high-grade glioma MYCN is frequently associated with Li-Fraumeni syndrome
por: Guerrini-Rousseau, Léa, et al.
Publicado: (2023) -
Clinical and molecular analysis of smoothened inhibitors in Sonic Hedgehog medulloblastoma
por: Pereira, Victor, et al.
Publicado: (2021)