Neurofibromatosis Type 1

What is Neurofibromatosis Type 1 (NF1)?

Neurofibromatosis Type 1 is a genetic condition that causes tumours to grow along the nerves. NF1 affects 1 in 3,000 newborns Symptoms may include pigmented spots on the skin, neurofibromas, or gelatinous masses in the iris. Other manifestations of the disorder include cardiovascular disease or hypertension. Those with NF1 are also at heightened risk for malignancies in cancer.

NF1 Research

Children and adolescents with neurofibromatosis type 1 (NF1) are at heightened risk for learning disabilities, attention difficulties and social-emotional challenges relative to same-aged peers. We are trying to understand which characteristics or behaviors contribute to poorer social competence in these populations and to design interventions to support better psychosocial adjustment in affected children. Dr. Pierpont and Dr. Hudock are developing an intervention curriculum for parents/caregivers of children with NF1 to help support families in coping with social-emotional concerns. We hope to make this intervention available to interested families in the near future!