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Legius syndrome

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Description

Legius syndrome is characterized by multiple café au lait macules without neurofibromas or other tumor manifestations of neurofibromatosis type 1 (NF1). Additional clinical manifestations reported commonly include intertriginous freckling, lipomas, macrocephaly, and learning disabilities / attention-deficit/hyperactivity disorder (ADHD) / developmental delays. Current knowledge of the natural history of Legius syndrome is based on the clinical manifestations of fewer than 300 individuals with a molecularly confirmed diagnosis; better delineation of the clinical manifestations and natural history of Legius syndrome will likely occur as more affected individuals are identified.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

255

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Genes

External Links

  • OMIM

    611431

  • Orphanet

    137605

  • HPO
  • Medgen

    C1969623

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