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Cutaneous neurofibromas in the genomics era: current understanding and open questions British Journal of Cancer Neurofibromatosis Type 1 is a genetic disorder characterized by multiple cutaneous neurofibromas, caf au lait macules, and systemic involvement due to NF1 gene mutation. Disclaimer For educational purposes only. Not medical advice. Consult a Neurofibromatosis: Types, Symptoms, Causes, and Treatments A newly developed therapeutic strategy offers potential in treating neurofibromatosis type 1 skin tumors Neurofibromatosis type 1 (NF 1) Lisch Nodules. EyeRounds.org: Online Ophthalmic Atlas
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