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Neurofibromatosis Program

At Children's Hospital of Philadelphia (CHOP), we recognize children with neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) require specialized care from pediatric experts who have extensive experience with these genetic disorders. You’ll find that high level of care at CHOP’s Neurofibromatosis Program. Our team works closely with your family, your pediatrician and your child's school to provide support and medical guidance for children with NF1 and NF2.

NF can affect multiple systems of the body. It can also cause learning or attention problems. Caring for your child with NF requires close monitoring and, when needed, medical procedures. Our program includes many specialists who care for all aspects of your child's health and well-being. We'll support your whole family every step of the way.

How we serve you

Our doctors, nurses and other experts are grouped into specially-trained treatment teams to give your child the best care. These teams give your child personalized care while building strong relationships to support your family.

Little boy at doctor appointment with his dad.

Meet your team

Your child will be cared for by one of the most accomplished teams of NF experts in the world. The team includes multiple subspecialties that include genetics, pediatrics, neuro-oncology, neuro-ophthalmology, ophthalmology and orthopedics.

Architectural detail of outside of building

Neurofibromatosis Program locations

Find locations where our experts treat children with NF.

Father and son smiling together looking at a laptop computer.

Neurofibromatosis Program resources

We have gathered resources to give you information and help you find answers to your questions. We hope this helps your family deal with any challenges you face.

Patient stories

Our Stories
Conor, 16, and his parents have been traveling to CHOP from South Carolina several times a year since he was an infant for NF1 treatment and clinical trials.
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