Genetic confirmation that ependymoma can arise as part of multiple endocrine neoplasia type 1 (MEN1) syndrome

Author:

Cuevas-Ocampo Areli K.,Bollen Andrew W.,Goode Benjamin,Pajtler Kristian W.,Chavez Lukas,Sharma Tanvi,Dai Sun-Chuan,McDermott Michael,Perry Arie,Korshunov Andrey,Solomon David A.ORCID

Funder

NIH Office of the Director

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Reference6 articles.

1. Al-Salameh A, Francois P, Giraud S (2010) Intracranial ependymoma associated with multiple endocrine neoplasia type 1. J Endocrinol Invest 33:353–356

2. Funayama T, Sakane M, Yoshizawa T et al (2013) Tanycytic ependymoma of the filum terminale associated with multiple endocrine neoplasia 1: first reported case. Spine J 13:e49–e54

3. Giraud S, Choplin H, Teh BT et al (1997) A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation. J Clin Endocrinol Metab 82:3487–3492

4. Kato H, Uchimura I, Morohoshi M et al (1996) Multiple endocrine neoplasia type 1 associated with spinal ependymoma. Intern Med 35:285–289

5. Kline CN, Joseph NM, Grenert JP et al (2016) Targeted next-generation sequencing of pediatric neuro-oncology patients improves diagnosis, identifies pathogenic germline mutations, and directs targeted therapy. Neuro-Oncol [Epub Nov 14]

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