Author:
Lu Yang,Wang Jingfu,Li Li,Zhang Xiaodong
Abstract
Abstract
Background
Cleidocranial dysplasia (CCD) is an autosomal dominant hereditary disorder. Besides skeletal abnormalities, CCD is often associated with dental complications, such as multiple supernumerary teeth and permanent teeth impaction or delayed eruption.
Methods
Supernumerary teeth of axial, sagittal and coronal CBCT view was characterized in detail and 3D image reconstruction was performed. Number and location of teeth, morphology of supernumerary teeth, positional relationship between supernumerary and adjacent permanent teeth, direction of supernumerary teeth in CCD patients were analyzed.
Results
The mean age of the 3 CCD patients in this study was 16.7 years. Among 36 supernumerary teeth, the majority of them were identified as apical side located and lingual side located. Normal orientation was the most common type in this study, followed by sagittal orientation, and horizontal orientation. Horizontal orientation teeth were all distributed in the mandible. Supernumerary teeth exhibited significantly shorter crown and dental-root lengths, as well as smaller crown mesiodistal and buccolingual diameters (P < 0.01). There was no difference in the number of supernumerary teeth between the maxilla and mandible, and the premolars region had the largest number of supernumerary teeth and the incisor region had the smallest number.
Conclusions
This study compares number and location of teeth, morphology of supernumerary teeth, positional relationship between supernumerary and adjacent permanent teeth and direction of supernumerary teeth, this study also provides a reference for the comprehensive evaluation of CCD patients before surgery.
Publisher
Springer Science and Business Media LLC
Reference28 articles.
1. Impellizzeri A, Midulla G, Romeo U et al. Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family [J]. Int J Dent, 2018, 2018: 6591414.
2. Listed N A. The classic: Marie, P., and Sainton P.: Sur la dysostose cleido-cranienne herediataire, Rev. neurol. 6:835, 1898. On hereditary cleido-cranial dysostosis [J]. Clinical Orthopaedics & Related Research. 1968, 58.
3. Jung Y J, Bae H S, Ryoo H M et al. A novel Runx2 mutation in exon 8, G462X, in a patient with cleidocranial dysplasia [J]. J Cell Biochem, 2017, 119(1).
4. Suda N, Hattori M, Kosaki K, et al. Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia [J]. Orthod Craniofac Res. 2010;13(4):197–202.
5. Jensen B L Kreiborgs. Development of the dentition in cleidocranial dysplasia [J]. J Oral Pathol Med. 1990;19(2):89–93.
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