Craniofacial and dentoalveolar morphology in individuals with Prader-Willi syndrome: a case-control study

Gisela Vasconcelos1, Jo S Stenehjem2,3, Stefan Axelsson4

  • 1TAKO-Centre, National Resource Centre for Oral Health in Rare Medical Conditions, Lovisenberg Diaconal Hospital, Pb 4970 Nydalen, 0440, Oslo, Norway. gisela.vasconcelos@tako.no.

Insights

Prader-Willi syndrome (PWS) affects craniofacial growth, with distinct patterns observed in children, young adults, and adults. Understanding these changes is crucial for dental treatment planning in individuals with PWS.

Area of Science:

  • Genetics and Developmental Biology
  • Orthodontics and Craniofacial Development
  • Pediatric Endocrinology

Background:

  • Prader-Willi syndrome (PWS) is a genetic disorder with diverse clinical manifestations including hypotonia, hyperphagia, obesity, and developmental delays.
  • Individuals with PWS often exhibit facial dysmorphology, orofacial dysfunction, and oral abnormalities, leading to severe tooth wear.
  • Limited information exists regarding craniofacial growth patterns and dental/skeletal relationships across different age groups in PWS patients.

Purpose of the Study:

  • To analyze craniofacial and dentoalveolar characteristics in individuals with PWS.
  • To investigate craniofacial growth direction in children, young adults, and adults with PWS.
  • To compare cephalometric data between PWS patients and a control group.

Main Methods:

  • Cephalometric analysis of lateral cephalograms from 42 individuals with genetically confirmed PWS.
  • Participants were categorized into three age groups: Children (<12 years), young adults (12-20 years), and adults (>20 years).
  • Cephalometric variables were compared between PWS patients and controls, stratified by age and sex.

Main Results:

  • Significant craniofacial pattern deviations were identified in all age groups of PWS patients compared to controls.
  • Children with PWS exhibited a retrognathic mandible (Class II) with posterior growth direction.
  • Adults with PWS displayed a prognathic mandible (Class III) with anterior growth direction and altered incisor positioning.

Conclusions:

  • The study reveals distinct age-dependent craniofacial growth patterns in Prader-Willi syndrome.
  • Findings highlight significant skeletal and dental differences compared to the general population.
  • This research provides valuable insights for planning orthodontic and prosthodontic treatments in PWS patients.
Abstract