Journals / Turkish Journal of Orthodontics / 2015 / Cilt: 28 - Sayı: 1

Orthodontic Care of Cleidocranial Dysplasia Patients

Pages
31–37
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The aim of this review is to discussthe history, genetic backgrounds, clinical and dental features, different dental treatment approaches and orthodonticmanagement of CCD. (Turkish J Orthod 2015;28:31–37)

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Cleidocranial dysplasia (CCD) is a rare congenital deformity inherited as an autosomal genetic trait with the prevalence of1:1,000,000.
📊
Key Findings & Data:It is characterized by dental defomities such as retained primary teeth, presence of supernumerary teeth, skeletaldicrepancy, malocclusion and retarded/absence of eruption of permanent teeth.
💡
Conclusion & Impact:The aim of this review is to discussthe history, genetic backgrounds, clinical and dental features, different dental treatment approaches and orthodonticmanagement of CCD. (Turkish J Orthod 2015;28:31–37)
🔬Design:Review & Systematic Survey
📍Scope:2015 Verileri
⚙️Variables:Domain Parameters

Abstract

Cleidocranial dysplasia (CCD) is a rare congenital deformity inherited as an autosomal genetic trait with the prevalence of1:1,000,000. It is characterized by dental defomities such as retained primary teeth, presence of supernumerary teeth, skeletaldicrepancy, malocclusion and retarded/absence of eruption of permanent teeth. The orthodontist take part in the team for patientswith CCD to resolve the eruption delay of permanent teeth and correct skeletal discrepancies. The aim of this review is to discussthe history, genetic backgrounds, clinical and dental features, different dental treatment approaches and orthodonticmanagement of CCD. (Turkish J Orthod 2015;28:31–37)

🔖

Cite This Article

YILMAZ, R. B. N., ÜLKÜR, F., NALBANTGİL, D. (2015). Orthodontic Care of Cleidocranial Dysplasia Patients. Turkish Journal of Orthodontics, Cilt: 28 - Sayı: 1, 31–37. https://ajindex.com/articles/375048

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. Park TKN, Vargervik K, Oberoi S. Orthodontic and surgical management of cleidocranial dysplasia. Korean J Orthod. 2013;43:248–260
  2. Farronato G, Maspero C, Farronato D, Gioventu S. Orthodontic treatment in a patient with cleidocranial dysostosis. Angle Orthod. 2009;79:178–185
  3. Bartsocas CS. Cleidocranial dysostosis in Homer. Archeia Ellin Pedia´tr Etair. 1973;36:107
  4. Bartsocas CS. Cleidocranial dysostosis in Homer. Archeia Ellin Pedia´tr Etair. 1973;36:107
  5. Beighton P, Sujansky E, Patzak B, Portele KA. Genetic skeletal dysplasias in the Museum of Pathological Anatomy, Vienna. Am J Med Genet. 1993;47:843–847
  6. Martin S. On natural displacement of the clavicle [in French]. J Me´ d Chir Pharmacol. 1765;23:456–460
  7. Marie P, Sainton P. Observation of hereditary hydrocephalus (father and son) by vice development of the skull and brain [in French]. Bull Soc Me´ d Hoˆ p Paris. 1897;14:706–712
  8. Hesse G. Other findings on dental system individual dysostosis [in German]. St Z Stomat. 1926;24:205
  9. Corona-Rivera JR, Romo-Huerta CO, Lo´ pez-Marure E, Ramos FJ, Estrada-Padilla SA, Zepeda-Romero LC. New ocular findings in two sisters with Yunis-Varon syndrome and literature review. Eur J Med Genet. 2011;54:76–81
  10. Mundlos S, Mulliken JB, Abramson DL, Warman ML, Knoll JHM, Olsen BR. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family. Hum Mol Genet. 1995;4:71–75
  11. Mundlos S, Otto F, Mundlos C, et al. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell. 1997;89:773–779
  12. A˚ berg T, Cavender A, Gaikwad JS, Bronckers AL, Wang X, et al. Phenotypic changes in dentition of RUNX2 homozygote-null mutant mice. J Histochem Cytochem. 2004;52: 131–139
  13. Suda N, Hattori M, Kosaki K, Banshodani A, Kozai K, Tanimoto K, et al. Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia. Orthod Craniofac Res. 2010;13:197–202
  14. Segal N, Puterman M. Cleidocranial dysplasia—review with an emphasis on otological and audiological manifestations. Int J Pediatr Otorhinolaryngol. 2007;71:523–526
  15. Chalala C, Noujeim ZEF, Chebel NA, Saade A. Multidisciplinary management of cleidocranial dysplasia. World J Orthod. 2014;4:31–39
  16. Yamamoto H, Sakae T, Davies JE. Cleidocranial dysplasia: a light microscope, electron microscope, and crystallographicstudy. Oral Surg Oral Med Oral Pathol. 1989;68:195– 200
  17. Jensen BL, Kreiborg S. Dental treatment strategies