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 Maddede Bu Makale
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Amaç & Hipotez:Cleidocranial dysplasia (CCD) is a rare congenital deformity inherited as an autosomal genetic trait with the prevalence of1:1,000,000.
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Temel Bulgular & Veri: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.
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Sonuç & Katkı: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)
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:2015 Verileri
⚙️Değişkenler:Alan Parametreleri
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)
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Bu Makaleye Atıf Yap
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
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
Martin S. On natural displacement of the clavicle [in French]. J Me´ d Chir Pharmacol. 1765;23:456–460
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
Hesse G. Other findings on dental system individual dysostosis [in German]. St Z Stomat. 1926;24:205
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
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
Mundlos S, Otto F, Mundlos C, et al. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell. 1997;89:773–779
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
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
Segal N, Puterman M. Cleidocranial dysplasia—review with an emphasis on otological and audiological manifestations. Int J Pediatr Otorhinolaryngol. 2007;71:523–526
Chalala C, Noujeim ZEF, Chebel NA, Saade A. Multidisciplinary management of cleidocranial dysplasia. World J Orthod. 2014;4:31–39
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
Jensen BL, Kreiborg S. Dental treatment strategies