Maxillonasal dysplasia (Binder syndrome): a lateral cephalometric assessment
Pubblicato online: 15 dic 2023
Pagine: 82 - 91
Ricevuto: 01 ago 2001
Accettato: 01 gen 2002
DOI: https://doi.org/10.2478/aoj-2002-0013
Parole chiave
© 2002 Barbara Carach et al., published by Sciendo
This work is licensed under the Creative Commons Attribution 4.0 International License.
Binder syndrome or maxillonasal dysplasia was first described by Binder in 1962, and is a disorder characterised by nasomaxillary hypoplasia. The records of 33 patients who had been diagnosed clinically with Binder syndrome at the Royal Children’s Hospital of Melbourne were examined. Of these 33 patients, 14 were selected because they met the inclusion criteria: that they had not had prior surgical and/or orthodontic treatment, and that high-quality lateral cephalometric radiographs were available. The craniofacial morphology of these patients was determined on lateral cephalometric radiographs and compared with published age- and sex-matched norms. In agreement with published studies, the anteroposterior lengths of the anterior cranial base and maxilla were reduced, and the majority of patients had a Class III skeletal relationship. Although the lower incisors tended to be prominent, both overjet and overbite fell within the ranges for the normal population. Despite the fact that the orthodontic and surgical treatment for patients with Binder syndrome is normally carried out within specialised units, clinicians should be aware of the variety of ways in which this condition may present.