Neurofibromatosis type 1 (NF1) is a genetic disorder characterized primarily by the development of multiple benign tumors called neurofibromas along nerves in the skin, brain, and other parts of the body. It is caused by a mutation in the NF1 gene, which is responsible for the production of neurofibromin, a protein that helps regulate cell growth. This condition manifests in various ways, including changes in skin coloring (café-au-lait spots), learning challenges, and skeletal abnormalities. NF
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May is NF (Neurofibromatosis) Awareness Month
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Have you ever wondered: What is NF1? It's short for neurofibromatosis type 1, but what IS it? You’re not alone — and we’re here to help. In the Big Questions about NF series, Kate Kelts, RN, BSN, breaks down key questions and concerns that NF patients and families ask most often. Missed the previous episodes? Check out our YouTube channel! 🎥 www.youtube.com/childrenstumor | Children's Tumor Foundation
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