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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 Typical manifestations of neurofibromatosis type 1 (NF1): caf au lait Download Scientific Diagram Cutaneous neurofibromas in the genomics era: current understanding and open questions British Journal of Cancer Pediatric low grade glioma models: advances and ongoing challenges Frontiers Neurofibromatosis 1 (NF1): Symptoms, Causes, Diagnosis, and More
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