ATRT-21. RHABDOID PREDISPOSITION SYNDROME: REPORT OF MOLECULAR PROFILES AND TREATMENT APPROACH IN THREE CHILDREN WITH SYNCHRONOUS ATYPICAL TERATOID/RHABDOID TUMOR AND MALIGNANT RHABDOID TUMOR

Abstract BACKGROUND Rhabdoid predisposition syndrome is characterized by germline alterations in SMARCB1 or SMARCA4, leading to synchronous or metachronous central nervous system (CNS) and extra-CNS rhabdoid tumors. Rare survivors have been reported to date. METHODS We describe the molecular profili...

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Veröffentlicht in:	Neuro-oncology (Charlottesville, Va.) Va.), 2020-12, Vol.22 (Supplement_3), p.iii280-iii280
Hauptverfasser:	Shatara, Margaret, Gupta, Ajay, Arja, Mohamed H Abu, Conley, Suzanne E, Patel, Priyal, Boué, Daniel R, Pierson, Christopher R, Thomas, Diana L, Meyer, Erin K, Shah, Summit H, Jones, Jeremy, Martin, Lisa, McAllister, Aaron, Schieffer, Kathleen M, Varga, Elizabeth A, Leraas, Kristen, Lichtenberg, Tara, LaHaye, Stephanie, Miller, Katherine E, Magrini, Vincent, Wilson, Richard K, Cottrell, Catherine E, Mardis, Elaine R, Aldrink, Jennifer H, Auletta, Jeffery J, Pindrik, Jonathan, Leonard, Jeffrey R, Osorio, Diana S, Finlay, Jonathan L, Ranalli, Mark, AbdelBaki, Mohamed S
Format:	Artikel
Sprache:	eng
Schlagworte:	Atypical Teratoid/Rhabdoid Tumors
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