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Neurofibromatosis, type 1

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Description

Neurofibromatosis 1 (NF1) is characterized by multiple café au lait spots, axillary and inguinal freckling, multiple cutaneous neurofibromas, iris Lisch nodules, and choroidal freckling. About half of people with NF1 have plexiform neurofibromas, but most are internal and not suspected clinically. Learning disabilities are present in at least 50% of individuals with NF1. Less common but potentially more serious manifestations include optic nerve and other central nervous system gliomas, malignant peripheral nerve sheath tumors, scoliosis, tibial dysplasia, and vasculopathy.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

3,804

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Genes

External Links

  • OMIM

    162200

  • Orphanet

    636

  • HPO
  • Medgen

    C0027831

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