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).
Cullen Mitchell has neurofibromatosis, a genetic disorder. His parents, Kelly and Ken, credit the Neurofibromatosis Program at CHOP with helping them manage the complexities of caring for a child with this condition.
Our Programs and Services
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.