Rare Disorders: Diagnosis and Therapeutic Planning for Patients Seeking Orthodontic Treatment
- PMID: 35329854
- PMCID: PMC8954363
- DOI: 10.3390/jcm11061527
Rare Disorders: Diagnosis and Therapeutic Planning for Patients Seeking Orthodontic Treatment
Abstract
The available literature on the orthodontic treatment of patients with rare disorders is extremely scarce. The aim of this study was to analyze the diagnosis and orthodontic treatment of a group of 94 individuals with rare diseases, referred for orthodontic evaluation to a university special care dentistry center (University of Santiago de Compostela, Spain). We created a control group of 94 systemically healthy individuals, paired by sex and age range. For all participants, we recorded their dental and skeletal abnormalities, oromotor dysfunctions and the characteristics of their orthodontic treatment. Some of the morphological and functional abnormalities were more prevalent in the rare disorders group than in the control group, including dental agenesis, microdontia, enamel defects, maxillary hypoplasia, overbite, cleft lip/palate, mouth breathing, atypical swallowing, lingual/labial interposition, labial incompetence, modified consistency diet, bruxism, and muscle tone abnormalities. Compared with the control group, the 56 patients with rare disorders who underwent orthodontic treatment required more desensitization sessions, used mixed appliances (fixed and removable) more often and for longer periods and had more frequent complications, such as gingivitis, caries, mucosal ulcers and recurrent debonding of the device. In conclusion, for selected patients with rare disorders, it is feasible to perform orthodontic treatment, whose planning will be determined by the dental-skeletal abnormalities and oromotor dysfunctions. Although complications are more frequent, they can typically be solved without having to stop treatment.
Keywords: dental care; dysgnathia; malocclusion; orofacial manifestations; orthodontics; rare diseases.
Conflict of interest statement
The authors declare no conflict of interest.
Similar articles
-
Oral mucosal complications in orthodontic treatment.Minerva Stomatol. 2019 Apr;68(2):84-88. doi: 10.23736/S0026-4970.18.04127-4. Minerva Stomatol. 2019. PMID: 30854838
-
FIXED OR REMOVABLE APPLIANCE FOR EARLY ORTHODONTIC TREATMENT OF FUNCTIONAL ANTERIOR CROSSBITE.Swed Dent J Suppl. 2015;(238):10-72. Swed Dent J Suppl. 2015. PMID: 26939312 Clinical Trial.
-
Orthodontic-care burden for patients with unilateral and bilateral cleft lip and palate.Dent Med Probl. 2020 Oct-Dec;57(4):411-416. doi: 10.17219/dmp/125874. Dent Med Probl. 2020. PMID: 33448166
-
Long-term skeletal stability after maxillary advancement with distraction osteogenesis using a rigid external distraction device in cleft maxillary deformities.Plast Reconstr Surg. 2004 Nov;114(6):1382-92; discussion 1393-4. doi: 10.1097/01.prs.0000138593.89303.1b. Plast Reconstr Surg. 2004. PMID: 15509923 Review.
-
The relationships between malocclusion, fixed orthodontic appliances and periodontal disease. A review of the literature.Aust Orthod J. 2007 Nov;23(2):121-9. Aust Orthod J. 2007. PMID: 18200790 Review.
Cited by
-
Axenfeld-Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report.Head Face Med. 2022 Jul 8;18(1):25. doi: 10.1186/s13005-022-00329-y. Head Face Med. 2022. PMID: 35804381 Free PMC article.
-
Dental Profile of Brazilian Patients with Rare Skeletal Genetic Disorders: Clinical Features and Associated Factors.Healthcare (Basel). 2024 May 19;12(10):1046. doi: 10.3390/healthcare12101046. Healthcare (Basel). 2024. PMID: 38786456 Free PMC article.
-
Three-Dimensional Analysis of the Maxillary Sinuses in Ancient Crania Dated to the V-VI Centuries BCE from Opi (Italy): Volumetric Measurements in Ancient Skulls from the Necropolis of Opi, Abruzzi, Italy.Diagnostics (Basel). 2024 Aug 3;14(15):1683. doi: 10.3390/diagnostics14151683. Diagnostics (Basel). 2024. PMID: 39125559 Free PMC article.
-
Oral Problems in Brazilian Individuals with Rare Genetic Diseases That Affect Skeletal Development.Int J Environ Res Public Health. 2024 Sep 18;21(9):1227. doi: 10.3390/ijerph21091227. Int J Environ Res Public Health. 2024. PMID: 39338110 Free PMC article.
-
Bone disease and oromaxillofacial disorders: a cross- sectional study in a Tanzanian pediatric population.Orphanet J Rare Dis. 2025 Feb 17;20(1):77. doi: 10.1186/s13023-025-03563-0. Orphanet J Rare Dis. 2025. PMID: 39962551 Free PMC article.
References
-
- The European Parliament and the Council of the European Union Regulation (EC) No 141/2000 of the European Parliament and of the Council of 16 December 1999 on Orphan Medicinal Products. [(accessed on 5 January 2022)]. Available online: http://ec.europa.eu/health/files/eudralex/vol-1/reg2000141cons-2009-07/r....
-
- EURORDIS Rare Diseases Europe. [(accessed on 5 January 2022)]. Available online: https://www.eurordis.org/es/enfermedades-raras.
-
- Elliott E.J., Zurynski Y.A. Rare diseases are a ‘common’ problem for clinicians. Aust. Fam. Physician. 2015;44:630–633. - PubMed
-
- Bloch-Zupan A. Manifestationsodontologiques des maladiesrares. Alphomenew. 2008;118:4–6.
LinkOut - more resources
Full Text Sources