Neurofibromatosis type 1 (NF1) is a genetic disorder characterized primarily by the development of multiple benign tumors called neurofibromas along nerves in the skin, brain, and other parts of the body. It is caused by a mutation in the NF1 gene, which is responsible for the production of neurofibromin, a protein that helps regulate cell growth. This condition manifests in various ways, including changes in skin coloring (café-au-lait spots), learning challenges, and skeletal abnormalities. NF
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