Rhabdoid Tumor Predisposition Syndrome: From Clinical Suspicion to General Management

Rhabdoid tumors are rare aggressive malignancies in infants and young children with a poor prognosis. The most common anatomic localizations are the central nervous system, the kidneys, and other soft tissues. Rhabdoid tumors share germline and somatic mutations in SMARCB1 or, more rarely, SMARCA4,...

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Detalles Bibliográficos
Autores principales: Del Baldo, Giada, Carta, Roberto, Alessi, Iside, Merli, Pietro, Agolini, Emanuele, Rinelli, Martina, Boccuto, Luigi, Milano, Giuseppe Maria, Serra, Annalisa, Carai, Andrea, Locatelli, Franco, Mastronuzzi, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937887/
https://www.ncbi.nlm.nih.gov/pubmed/33692948
http://dx.doi.org/10.3389/fonc.2021.586288

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937887/
https://www.ncbi.nlm.nih.gov/pubmed/33692948
http://dx.doi.org/10.3389/fonc.2021.586288

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