Occlusal Relations in Patients With Scaphocephaly
Ariane Lebuis1, Patricia Bortoluzzi, Nelly Huynh
1*Faculty of Dentistry, Université de Montréal †Craniofacial Surgery Clinic, Centre Hospitalier Universitaire Ste-Justine, Montreal, Quebec, Canada.
Insights
Scaphocephaly, a condition from premature sagittal suture fusion, shows more clinical Class II malocclusions in children. However, radiographic measurements and corrective surgery do not significantly impact occlusion.
Area of Science:
- Craniofacial Surgery
- Orthodontics
- Pediatric Dentistry
Background:
- Scaphocephaly results from premature sagittal suture fusion, often treated with surgery in infancy.
- No prior data exists on occlusion in scaphocephalic patients or surgery's effect.
Purpose of the Study:
- To describe occlusion in scaphocephalic patients.
- To compare scaphocephalic occlusion with the general pediatric population.
- To compare occlusion between surgically treated and untreated scaphocephalic subgroups.
Main Methods:
- Orthodontic assessment of 91 scaphocephalic patients (2-11 years).
- Comparison of clinical and cephalometric data between operated (n=44) and unoperated (n=47) groups.
- Lateral cephalometric radiography for 38 patients.
Main Results:
- Scaphocephalic patients showed a higher prevalence of clinical Class II malocclusions.
- Cephalometric values for skeletal Class II malocclusions remained within normal limits.
- Maxillary width was within normal limits; surgery did not affect occlusion.
Conclusions:
- Scaphocephalic patients exhibit more clinical Class II malocclusions but normal skeletal and transverse dimensions.
- Craniovault surgery for scaphocephaly does not negatively impact occlusion.
Abstract:
Scaphocephaly results from a premature fusion of the sagittal suture. Usually, cranial vault corrective surgery is performed during the first year of life. There is currently no scientific data regarding occlusion of scaphocephalic patients, or the potential effect of craniovault surgery on the occlusion. The aims were to describe occlusion in scaphocephalic patients and compare with a general pediatric population, and to compare the difference in occlusion of surgically versus unoperated treated scaphocephalic subgroup. A total of 91 scaphocephalic patients (71 boys aged between 2 and 11 y) seen at the Craniofacial Clinic of CHU Ste-Justine's formed the experimental group. All patients received an orthodontic assessment. Among them, 44 underwent craniovault surgery, whereas 47 remained unoperated. Thirty-eight (33 boys; 17 operated) had lateral cephalometric radiographies, some of them also had cephalometric growth follow-ups. Clinical values for dental classification and overjet indicate an increased prevalence of class II malocclusions in scaphocephalic patients. However, interestingly enough, cephalometric values indicative of skeletal class II malocclusions (ie, N-A perp HP, N-B perp HP, N-Pog perp HP, Wits, N-A-Pog) remained within normal limits. Some cephalometric values present statistically significant differences between operated and unoperated patients (ANS-PNS t2, P = 0.025; /1-FH t2, P = 0.028), but these are individual variations not related to scaphocephaly. Maxillary width of scaphocephalic children remains within normal limits. Scaphocephalic patients clinically presented more class II malocclusions compared with normal children. Radiographic values remain, however, within normal limits for both anteroposterior and transverse dimensions. Corrective craniovault surgery did not affect occlusion in these patients.
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