Category: Genetic Disorders / Neurocutaneous Syndromes
Neurofibromatosis Type 1 (NF1) is a common genetic disorder caused by a mutation in the NF1 gene, characterized by multiple café-au-lait spots, neurofibromas, Lisch nodules, and an increased risk of tumors.
Estimated at 1 in 3,000 live births worldwide (Source: National Institute of Neurological Disorders and Stroke).
Discover the latest clinical trials and treatments for Neurofibromatosis Type 1 on JourneyForHealth.
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