Neurofibromatosis Program

Our team at the Neurofibromatosis Program works closely with your family, community pediatricians, and schools to provide support and medical guidance for children with the genetic disorders neurofibromatosis type 1 (NF1) and type 2 (NF2).

Neurofibromatosis Type 1: Cullen’s Story

Our Team

The Neurofibromatosis Program's team of experts includes dedicated physicians as well as those from multiple subspecialties, including genetics, pediatrics, neuro-oncology, neuro-ophthalmology, ophthalmology and orthopedics.