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Tumors of central and peripheral nervous system associated with inherited genetic syndromes.

Abstract
There are several genetic syndromes that predispose to the development of tumors of the nervous system. In the present study, we provide a review of the tumors that are associated with neurofibromatosis type 1, neurofibromatosis type 2, tuberous sclerosis complex, von Hippel-Lindau disease, Li-Fraumeni syndrome, Cowden disease, Turcot syndrome, nevoid basal cell carcinoma syndrome (Gorlin syndrome) and rhabdoid predisposition syndrome, which are the most common.
AuthorsKalliopi Stefanaki, George A Alexiou, Christina Stefanaki, Neofytos Prodromou
JournalPediatric neurosurgery (Pediatr Neurosurg) Vol. 48 Issue 5 Pg. 271-85 ( 2012) ISSN: 1423-0305 [Electronic] Switzerland
PMID23796843 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2013 S. Karger AG, Basel.
Topics
  • Animals
  • Brain Neoplasms (diagnosis, epidemiology, genetics)
  • Central Nervous System Neoplasms (diagnosis, epidemiology, genetics)
  • Colorectal Neoplasms (diagnosis, epidemiology, genetics)
  • Humans
  • Li-Fraumeni Syndrome (diagnosis, epidemiology, genetics)
  • Neoplastic Syndromes, Hereditary (diagnosis, epidemiology, genetics)
  • Neurofibromatosis 1 (diagnosis, epidemiology, genetics)
  • Peripheral Nervous System Neoplasms (diagnosis, epidemiology, genetics)
  • Syndrome
  • Tuberous Sclerosis (diagnosis, epidemiology, genetics)
  • von Hippel-Lindau Disease (diagnosis, epidemiology, genetics)

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