Palatoplasty for the Patient With Campomelic Dysplasia-Report of a Case and Review of the Literature

Cleft Palate Craniofac J. 2022 Jan;59(1):132-136. doi: 10.1177/1055665621992654. Epub 2021 Feb 12.

Abstract

Campomelic dysplasia (CMPD) is a skeletal disorder resulting from SOX9 gene mutations. Palatoplasty is rare due to a high lethality rate in infants from respiratory distress. Our patient had characteristic symptoms of CMPD, including short bowed limbs, macrocephaly, low-set ears, short palpebral fissures, hypertelorism, a flat nasal bridge, a long philtrum, micrognathia, and a cleft palate. We performed a Furlow palatoplasty when the patient was 2 years 9 months of age, after respiratory conditions had stabilized. We reviewed the literature of CMPD cases that underwent palatoplasty and discussed the optimal timing and surgical methods.

Keywords: Furlow palatoplasty; campomelic dysplasia; cleft palate.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Campomelic Dysplasia* / diagnostic imaging
  • Campomelic Dysplasia* / surgery
  • Cleft Palate* / surgery
  • Disorders of Sex Development*
  • Humans
  • Infant
  • Palate, Soft / surgery
  • Plastic Surgery Procedures*
  • Retrospective Studies
  • Treatment Outcome
  • Velopharyngeal Insufficiency*