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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Publicat a:Neuro Oncol
Autors principals: El-Ayadi, Moatasem, Ansari, Marc, Kühnöl, Caspar, Bendel, Anne, Sturm, Dominik, Pietsch, Torsten, Kramm, Christof, von Bueren, André
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2017
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Accés en línia: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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