Understanding NF1: Causes, Symptoms, and Management

Jan 01, 2026

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Neurofibromatosis type 1 (NF1) is a genetic disorder characterized by the development of numerous tumors on nerves, skin changes, and bone deformities. This condition is caused by mutations in the NF1 gene, which plays a crucial role in regulating cell growth. Symptoms may include café-au-lait spots, neurofibromas, and learning disabilities. Effective management involves regular monitoring, surgical interventions for tumor removal, and supportive therapies for associated symptoms. Genetic counseling is also recommended for affected families.

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Understanding NF1: Causes, Symptoms, and Management

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