Neurofibromatosis type 2 is most often diagnosed based on the presence of physical symptoms that are part of the specific diagnostic criteria for the disorder. Genetic testing for the NF2 mutation is ...

This change was based on the results of an international effort, sponsored by the Children’s Tumor Foundation (CTF), to review and update the diagnostic criteria of neurofibromatosis to include the ...

Meningiomas, often linked to the loss of the NF2 gene, are a hallmark of NF2-SWN ... they will need to undergo several phases of complex testing and no model exists to look at these therapies ...

Prof Palaniandy said Neurofibromatosis is a genetic condition with three conditions - Neurofibromatosis type 1 (NF1), Neurofibromatosis type 2 (NF2) and Schwannomatosis involving the development ...