Craniofacial Syndromes: Etiology, Impact and Treatment

Ching Fang Chang, Elizabeth N. Schock, David A. Billmire, Samantha A. Brugmann

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

3 Scopus citations

Abstract

The craniofacial complex is derived from seven separate embryonic swellings (paired maxillary, mandibular and lateral nasal prominences and a singular frontonasal prominence) that grow and fuse together to form a seamless face. The craniofacial complex is derived from tissues of all embryonic origins including ectoderm, neural crest, mesoderm, and endoderm. The most common craniofacial defects affect the growth and development of first arch structures (maxillary and mandibular prominences) and the development of the oral cavity. Midline defects are caused by aberrant growth and development of the frontonasal prominence. Midline defects are among the most difficult to repair because they often involve not only cranial bones and soft tissue, but also the brain.

Original languageEnglish
Title of host publicationPrinciples of Developmental Genetics
Subtitle of host publicationSecond Edition
Pages653-676
Number of pages24
DOIs
StatePublished - 2015

Bibliographical note

Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.

Keywords

  • Ciliopathies
  • Craniofacial
  • Craniosynostosis
  • Holoprosencephaly
  • Miller/Nager syndrome
  • Neural crest cells
  • Opitz BBB
  • Treacher Collins

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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