Neurofibromatosis Report

NeurofibromatosisNeurofibromatosis is a hereditary condition characterized by the onset of benign tumors, called neurofibromas, along the course of the nerves. The two main types differ clinically and genetically, although they belong to the same nosological entity. The genetic alterations underlying Neurofibromatosis compromise the tumor suppressor function of the genes involved, thus opening the way to uncontrolled cell proliferation.5 genes analyzed It is recommended if: This report supports the diagnosis of Neurofibromatosis, which generally occurs in adulthood, but is also useful for those who have a positive family history for the pathology (this is the main risk factor). List of main conditions: Neurofibromatosis type 1/2 Schwannomatosis