Unveiling the complexity of neurofibromatosis type 1: Innovations in genetic understanding and clinical management. A narrative review
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Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder caused by mutations in the NF1 gene. The most important signs are café-au-lait spots, intertriginous freckling, and neurofibromas. The disease has a progressive course, the penetrance is almost ... ...
