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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 A newly developed therapeutic strategy offers potential in treating neurofibromatosis type 1 skin tumors The Neurofibromatoses Plastic Surgery KeyPlastic Surgery Key Typical manifestations of neurofibromatosis type 1 (NF1): caf au lait Download Scientific Diagram Neurofibromatosis 1 (NF1): Symptoms, Causes, Diagnosis, and More Neurofibromatosis Treatment & Management Point of Care StatPearls
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