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Posterior fossa tumors in children with neurofibromatosis type 1 (NF1)

✍ Scribed by Ignacio Pascual-Castroviejo; Samuel I. Pascual-Pascual; Juan Viaño; Fernando Carceller; Manuel Gutierrez-Molina; Carmen Morales; Remedios Frutos-Martinez

Publisher
Springer
Year
2010
Tongue
English
Weight
309 KB
Volume
26
Category
Article
ISSN
0256-7040

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## Abstract Neurofibromatosis Type 1 (NF1) is a frequent tumor suppressor gene disorder characterized by multiple benign tumors and high risk of malignancy. Internal tumor burden is a major disease‐associated manifestation and can be most adequately assessed by magnetic resonance imaging of the who