Neurofibromatosis in Neurological Practice (Description of a Clinical Case of Neurofibromatosis 2nd Type)

Abstract

Neurofibromatosis is a complex genetic disorder with multiple symptoms and significant phenotypic variability. The most severe is second type of neurofibromatosis. It characterizes by tumors of central and peripheral nervous system. The article describes a complex clinical case of neurofibromatosis type 2. Such a clinical case in neurological practice can be found infrequently. The complexity of diagnosis and treatment of these diseases requires a coordinated multidisciplinary approach.