Apert Syndrome

Apert syndrome clinical presentation

Etiology:

Genetic disorder – Premature fusion of certain skull bones (craniosynostosis) – skull does not grow normally – affects shape of head and face

Clinical:

1. Skeletal abnormalities:

  • Syndactyly
  • Acrocephaly
  • Brachicephaly

2. Oral complications:

  • High palatal vault
  • Posterior palatal cleft and bifid uvule
  • Multiple impactions and malocclusions

3. Ovoid skull + horizontal supra-orbital groove

4. Early closure of coronal & sagittal sutures

  • Mid third face underdeveloped
  • Patent alveolar & frontal sutures

Treatment:

Surgery

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