LINC-16. MEDULLOBLASTOMA IN A BOY WITH RUBINSTEIN-TAYBI SYNDROME: A CASE REPORT

BACKGROUND: Rubinstein–Taybi syndrome (RTS) is characterized by multiple congenital anomalies and associated with mutations in CREBBP (70%) and EP300 (5–10%). Previous reports have suggested an increased incidence of benign and possibly also malignant tumors, but the correlation remains unclear. Her...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Neuro Oncol
Päätekijät: del Campo, Regina M Navarro-Martin, Soto-Mancilla, Juan Luis, Arredondo-Navarro, Luis A, Orozco-Alvarado, Ana L, Sanchez-Zubieta, Fernando A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2020
Aiheet:
Pediatric Neuro-Oncology in Asia and other Low/Middle Income Countries
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7715788/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa222.451
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