EPID-18. NOONAN SYNDROME CAN BE ASSOCIATED WITH HIGH GRADE GLIOMA; A REPORT OF TWO CASES

Noonan syndrome (NS), an autosomal dominant disorder, is characterized by short stature, congenital heart defects, developmental delay, and facial dysmorphism. PTPN11 germline mutations are the most common cause of NS. Patients with NS are at an increased risk of developing hematologic malignancies...

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Detalhes bibliográficos
Publicado no:Neuro Oncol
Main Authors: El-Ayadi, Moatasem, Ansari, Marc, Kühnöl, Caspar, Bendel, Anne, Sturm, Dominik, Pietsch, Torsten, Kramm, Christof, von Bueren, André
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5692500/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/nox168.295
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