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The document discusses various phacomatoses, including Neurofibromatosis types 1 and 2, Tuberous Sclerosis, and Sturge-Weber Syndrome, detailing their definitions, incidence, clinical features, and treatment options. Neurofibromatosis is characterized by skin lesions and neurological complications, while Tuberous Sclerosis involves hamartomas in multiple organs and significant neurological symptoms. Sturge-Weber Syndrome presents with facial angiomas and neurological deficits, with treatments primarily focu

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n5b6t5gswt

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EN