Abstract
The two common types of neurofibromatosis (NF) are genetically and clinically distinct diseases, each of which promotes the growth of neurofibromas and schwannomas that arise in the myelin nerve sheaths of peripheral or cranial nerves. Other tumors may arise from a variety of tissues including meningiomas, optic gliomas, and ependymomas. Both NF1 (chromosome 17q) and NF2 (chromosome 22q) are dominantly transmitted, with half of cases arising from new mutations. Diagnostic criteria for NF1 and NF2 have been developed by consensus.1 Physical features and neuroimaging of NF are shown in figures 1 and 2 …
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.