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Neurofibromatosis type 1 is an autosomal dominant genetic disorder that may present in patients as café au lait spots, Lisch nodules, neurofibromas, optic glioma, pheochromocytoma, and bone abnormalities.

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Nuances of Syndromic Scoliosis: Neurofibromatosis Type 1

  • 章节

  • 发表日期：

    2026年

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  • Zaid Elsabbagh,
  • Paul Sponseller

摘要

Neurofibromatosis type 1 is an autosomal dominant genetic disorder that may present in patients as café au lait spots, Lisch nodules, neurofibromas, optic glioma, pheochromocytoma, and bone abnormalities.