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Key terms: caused bone gene neurofibroma ras lesions tumors protein limb manifests arise arm growth patients disorder optic spine dura chromosome neurofibromin kinase tissue chronic develop surgery learning clinical mutation skeletal most common diagnosis genetic imaging au lait schwannoma been shown complications symptoms peripheral nerve plexiform neurofibroma neurofibromatosis malignant dysplasia scoliosis cutaneous cognitive problems autosomal dominant von recklinghausen magnetic resonance peripheral nervous system Search external links cited by footnotes on Wikipedia page Neurofibromatosis type I: |
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