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Achondroplasia

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Description

Achondroplasia is the most common cause of disproportionate short stature. Affected individuals have rhizomelic shortening of the limbs, macrocephaly, and characteristic facial features with frontal bossing and midface retrusion. In infancy, hypotonia is typical, and acquisition of developmental motor milestones is often both aberrant in pattern and delayed. Intelligence and life span are usually near normal, although craniocervical junction compression increases the risk of death in infancy. Additional complications include obstructive sleep apnea, middle ear dysfunction, kyphosis, and spinal stenosis.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

17

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Genes

External Links

  • OMIM

    100800

  • Orphanet

    15

  • HPO
  • Medgen

    C0001080

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