Robin Sequence Facial Profile After Conservative Treatment: A Long-Term Follow-Up

Author:

Siqueira Gabriela Leticia Clavisio1,Tonello Cristiano2ORCID,Peixoto Adriano Porto3,Daskalogiannakis John4,Garib Daniela Gamba5,Marques Ilza Lazarini2,Ceide Roseli Zechi3,Alonso Nivaldo2,Ozawa Terumi Okada3

Affiliation:

1. PhD student, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo

2. Hospital Department, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo

3. Department of Orthodontics, Hospital for Rehabilitation of Craniofacial Anomalies-University of São Paulo (HRAC-USP), Bauru, SP, Brazil

4. Department of Orthodontics, University of Toronto and Department of Dentistry, The Hospital for Sick Children, Toronto, Ontario, Canada

5. Department of Orthodontics, Bauru School of Dentistry and Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, SP, Brazil

Abstract

Introduction: Robin sequence (RS) is a congenital clinical condition characterized by micrognathia, glossoptosis, and respiratory distress. Conservative methods could be responsible for releasing feeding and respiratory impairment but little information about mandibular growth is known in long-term follow-up. Objective: Assessing the longitudinal behavior of the facial profile of individuals with isolated RS who underwent conservative micrognathia treatment using photographs during the whole craniofacial growth. Methods: Photographs of the right facial profile of 100 patients were used (50 individuals with isolated RS and 50 individuals without craniofacial anomaly). The individuals with RS were evaluated at 3 different times (T1: infant, T2: mixed dentition, T3: permanent dentition) by measuring the facial convexity angle (FCA; G.Sn.Pog´). A comparison between T3 and control group (C), individuals without craniofacial anomalies and in permanent dentition, was also performed, checking the FCA, nasolabial angle (Ls.Sn.Cm), mentolabial fold (Li.Si.Pog´), facial inferior third (Sn.Gn´.C) angles and the ratio between middle anterior facial height and lower anterior facial height. Results: The T3 group showed an increased angle of facial convexity and increased facial inferior third angle and middle anterior facial height/lower anterior facial height ratio compared with the control group. In the longitudinal evaluation of individuals with isolated RS, significant differences were identified between T1 and T2 groups and T1 and T3 groups showing that the increased facial convexity was higher in the infants and that did not change significantly between the phases of mixed and permanent dentition. Conclusions: RS showed increased facial convexity in all phases evaluated, but their convexity decreased with growth. When compared with individuals without craniofacial anomalies, the individuals continue to exhibit retrognathism in the permanent dentition. The lack of a mandible projection has led to a considerable number of orthognathic surgeries for the correction of discrepancies.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference22 articles.

1. Best practices for the diagnosis and evaluation of infants with Robin sequence: a clinical consensus report;Breugem;JAMA Pediatr,2016

2. Airway obstruction after lingual frenulectomy in two infants with Pierre Robin sequence;Genther;Int J Pediatr Otorhinolaryngol,2015

3. The Robin anomalad—its nonspecificity and associated syndromes;Cohen;J Oral Surg,1976

4. Facial profile evaluation of isolated Pierre Robin Sequence;Ozawa;Cleft Palate Craniofac J,2012

5. Growth of mandible in infants with micrognathia;Pruzansky;Am J Dis Child,1954

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