Neurofibromatosis Type 1: Causes, Symptoms & Treatment
Neurofibromatosis type 1 is a genetic disorder for which malformations of the central nervous system and skin are characteristic. With approximately one in 3000 newborns, neurofibromatosis type 1 is one of the most common genetic disorders. What is neurofibromatosis type 1? Neurofibromatosis type 1 (also known as Recklinghausen’s disease) is a genetic phakomatosis with malformations … Neurofibromatosis Type 1: Causes, Symptoms & Treatment