Contents: NF2 -- An autosomal dominant inherited tumours predisposition syndrome -- Bilateral vestibular schwannomas -- Schwannomas of other cranial and spinal nerve routes -- Meningiomas -- Ependymomas affected mainly the upper spine -- Cataracts -- Mutations in the NF2 gene Gorlin syndrome -- An autosomal dominant inherited tumours predisposition syndrome -- Multiple BCCs -- Jaw keratocysts -- Medulloblastoma -- Mutations in the PTCH gene
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Animated audio-visual presentation with synchronized narration
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