Complex dental anomalies in a belatedly diagnosed cleidocranial dysplasia patient |
Lu, Hui
(Guanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-Sen University)
Zeng, Binghui (Department of Medical Genetics, Zhongshan School of Medicine and Center for Genome Research, Sun Yat-Sen University) Yu, Dongsheng (Guanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-Sen University) Jing, Xiangyi (Department of Medical Genetics, Zhongshan School of Medicine and Center for Genome Research, Sun Yat-Sen University) Hu, Bin (Department of Medical Genetics, Zhongshan School of Medicine and Center for Genome Research, Sun Yat-Sen University) Zhao, Wei (Guanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-Sen University) Wang, Yiming (Department of Medical Genetics, Zhongshan School of Medicine and Center for Genome Research, Sun Yat-Sen University) |
1 | Ott CE, Leschik G, Trotier F, Brueton L, Brunner HG, Brussel W, et al. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Hum Mutat 2010; 31: E1587-93. DOI |
2 | Karsenty G. Update on the transcriptional control of osteoblast differentiation. Bonekey Osteovision 2007; 4: 164-70. DOI |
3 | Camilleri S, McDonald F. Runx2 and dental development. Eur J Oral Sci 2006; 114: 361-73. DOI |
4 | McNamara CM, O'Riordan BC, Blake M, Sandy JR. Cleidocranial dysplasia: radiological appearances on dental panoramic radiography. Dentomaxillofac Radiol 1999; 28: 89-97. DOI |
5 | Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama K. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2: possible involvement of non-genetic or epigenetic regulation. Orthod Craniofac Res 2007; 10: 222-5. DOI |
6 | Kolokitha OE, Ioannidou I. A 13-year-old Caucasian boy with cleidocranial dysplasia: a case report. BMC Res Notes 2013; 6: 6. DOI |
7 | Wang XP, Fan J. Molecular genetics of supernumerary tooth formation. Genesis 2011; 49: 261-77. DOI |
8 | Chang JY, Wang JT, Wang YP, Liu BY, Sun A, Chiang CP. Odontoma: a clinicopathologic study of 81 cases. J Formos Med Assoc 2003; 102: 876-82. |
9 | Rajab LD, Hamdan MA. Supernumerary teeth: review of the literature and a survey of 152 cases. Int J Paediatr Dent 2002; 12: 244-54. DOI |
10 | Adaki SR, Yashodadevi BK, Sujatha S, Santana N, Rakesh N, Adaki R. Incidence of cystic changes in impacted lower third molar. Indian J Dent Res 2013; 24: 183-7. DOI |
11 | Muthukumar RS, Arunkumar S, Sadasiva K. Bilateral fusion of mandibular second premolar and supernumerary tooth: a rare case report. J Oral Maxillofac Pathol 2012; 16: 128-30. DOI |
12 | Tsujino K, Yonezu T, Shintani S. Effects of different combinations of fused primary teeth on eruption of the permanent successors. Pediatr Dent 2013; 35: E64-7. |
13 | Callea M, Bellacchio E, Di Stazio M, Fattori F, Bertini E, Yavuz I, et al. A case of cleidocranial dysplasia with peculiar dental features: pathogenetic role of the RUNX2 mutation and long term follow-up. Oral Health Dent Manag 2014; 13: 548-51. |
14 | Park TK, Vargervik K, Oberoi S. Orthodontic and surgical management of cleidocranial dysplasia. Korean J Orthod 2013; 43: 248-60. DOI |
15 | Saracoglu U, Kurt B, Gunhan O, Guven O. MIB-1 expression in odontogenic epithelial rests, epithelium of healthy oral mucosa and epithelium of selected odontogenic cysts. An immunohistochemical study. Int J Oral Maxillofac Surg 2005; 34: 432-5. DOI |
16 | Mundlos S. Cleidocranial dysplasia, clinical and molecular genetics. J Med Genet 1999; 36: 177-82. |
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