Syndromic Craniofacial Disorders

Robert J Tibesar; Andrew R Scott

doi:10.1016/j.fsc.2023.07.002

Syndromic Craniofacial Disorders

Facial Plast Surg Clin North Am. 2024 Feb;32(1):141-156. doi: 10.1016/j.fsc.2023.07.002. Epub 2023 Aug 23.

Authors

Robert J Tibesar¹, Andrew R Scott²

Affiliations

¹ Pediatric ENT and Craniofacial Surgery, Children's Hospital Minnesota, 2530 Chicago Avenue South CSC 450, Minneapolis, MN 55404, USA. Electronic address: Robert.Tibesar@childrensmn.org.
² Pediatric ENT and Craniofacial Surgery, Tufts Medical Center, Floating Building, 6th Floor, 755 Washington Street Box 850, Boston, MA 02111, USA.

PMID: 37981410
DOI: 10.1016/j.fsc.2023.07.002

Abstract

This article reviews the most common craniofacial syndromes encountered in clinical practice. Key physical features of each condition are highlighted to aid in accurate recognition and diagnosis. Optimal individualized treatment approaches are discussed.

Keywords: Apert; Craniofacial syndromes; Crouzon; Hemifacial microsomia; Muenke; Pfeiffer; Saethre-chotzen; Syndromic craniosynostosis.

Publication types

Review

MeSH terms

Humans
Physical Examination*
Syndrome