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Managing Neurofibromatosis Type 1: Emerging Therapies and Clinical Advances
Neurofibromatosis Type 1 (NF1) is one of the most common inherited neurological disorders, affecting approximately 1 in 3,000 individuals worldwide. Caused by mutations in the NF1 gene, it manifests as a multisystem disorder characterized by pigmentary changes, tumor growth, and neurodevelopmental challenges. NF1 is typically diagnosed in childhood and presents a highly variable clinical...
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