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Key terms: approximately arise autosomal dominant been shown bone brain caused chronic cognitive problems complications cutaneous develop diagnosis disease disorder dura dysplasia gene growth imaging increased individuals lesions limb magnetic resonance malignant manifests most common mutation neurofibroma neurofibromatosis optic patients peripheral nerve peripheral nervous system plexiform neurofibroma schwannoma scoliosis severe skeletal solitary spine structures surgery symptoms tumors von recklinghausen Search external links cited by footnotes on Wikipedia page Neurofibromatosis type I: |
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