Abstract
This chapter contains examples of common dental anomalies, as encountered in pediatric dental practice, which were not treated in Chap. 6. The radiographic images taken with different radiographic techniques and their radiographic differential diagnoses are presented. The aim of this chapter is to familiarize the reader with the different results of the techniques explained in the previous chapters. Obviously not all types of anomalies were captured in this textbook chapter, but at least the reader will get a better feel about how the images turn out and what information can be retrieved from them.
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Further Reading
Alhilou A, Beddis HP, Mighell AJ, Durey K. Dentin dysplasia: diagnostic challenges. BMJ Case Rep. 2018; https://doi.org/10.1136/bcr-2017-223942.
Al-Tuwirqi A, Lambie D, Seow WK. Regional odontodysplasia: literature review and report of unusual case located in the mandible. Ped Dent. 2014;36:62–7.
Andersson K, Malmgren B, Astrom E, Dahllof G. Dentinogenesis imperfecta type II in Swedish children and adolescents. Orphanet J Rare Dis. 2018;13(145) https://doi.org/10.1186/s13023-018-0887-2.
Bloch-Zupan A, Huckert M, Stoetzel C, Meyer J, Geoffrey V, Razafindrakoto RW, Dollfus H. Detection of a novel DSPP mutation by NGS in a population isolate in Madagascar. Front Physiol. 2017;7:70. https://doi.org/10.3389/fphys.2016.00070.
Cawson RA, Odell EW. Cawson’s essentials of oral pathology and oral medicine. 8th ed. London: Churchill Livingstone Elsevier.
Chen D, Li X, Lu F, Wang Y, Xiong F, Li Q. Dentin dysplasia type I – a dental disease with genetic heterogeneity. Oral Dis. 2018;. 10.111/odi.12861
Daryani D, Nair G, Naidu G. Dentin dysplasia type II: an exclusive report of two cases in siblings. J Indian Ac Oral Med Rad. 2017:132.
De Rio EP, Sir-Mendoza FJ, Carbal-Gonzalez AC. Odontomas: report and clinical case series. School of Dentistry, University of Cartagena, 2010-2015. Revista Odontologica Mexicana. 2017;21:e208–11.
De Sa Cavalcante D, Fonteles CSR, Ribeiro TR, Kurita LM, de Pimenta AVM, Carvalho FSR, Costa FWG. Mandibular regional odontodysplasia in an 8 year old boy showing teeth disorders, gubernaculum tracts, and altered bone fractal pattern. Int J Clin Ped Dent. 2018;11(2):128–34.
Gasse B, Prasad M, Delgado S, Huckert M, Kawczynski M, Garret-Bernardin A, Lopez-Cazaux S, Bailleil-Forestier I, Maniere M-C, Stoetzel C, Bloch-Zupan A, Sire J-Y. Evolutionary analysis predicts sensitive positions of MMP20 and validates newly- and previously- identified MMP20 mutations causing amelogenesis imperfecta. Front Physiol. 2017;8:398. https://doi.org/10.3389/fphys.2017.00398.
Kammoun R, Behets C, Mansour L, Ghoul-Mazgar S. Mineral features of connective dental hard tissues in hypoplastic amelogenesis imperfecta. Oral Dis. 2018;24:384–92.
Kim YJ, Kang J, Seymen F, Koruyucu M, Gencay K, Shin TJ, Hyun H-K, Lee ZH, Hu JC-C, Simmer JP, Kim J-W. Analysis of MMP20 missesnse mutations in two families with hypomaturation amelogenesis imperfecta. Front Physiol. 2017;8:229. https://doi.org/10.3389/fphys.2017.00229.
Kim Y, Seymen F, Kang J, Koruyucu M, Tuloglu N, Bayrak S, Tuna EB, Lee ZH, Shin TJ, Hyun H-K, Lee S-H, Hu J, Simmer J, Kim J-W. Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta. Clin Oral Invest. 2018; https://doi.org/10.1007/s00784-018-2577-9.
Li F, Liu Y, Yang J, Zhang F, Oral FH. Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia. Dis. 2017;23:360–6.
Neville D, Allen B. Oral and maxillofacial pathology. 2nd ed. Philadelphia: Saunders.
Rajasekharan S, Martens L, Vanhove C, Aps J. In vitro analysis of extracted dens invaginatus teeth using various radiographic imaging techniques. Eur J Paediatr Dent. 2014;15:265–70.
Smith MH, Cohen DM, Katz J, Bhattacharyya I, Islam NM. Segmental odontomaxillary dysplasia. An unrecognized entity. JADA. 2018;149(2):153–62.
Taleb K, Lauridsen E, Daugaard-Jensen J, Nieminen P, Kreiborg S. Dentinogenesis imperfecta type II-genotype and phenotype analysis in three Danish families. Mol Genet Genomic Med. 2018;6:339–49.
Umapathy T, Veena A, Nagarathna C, Rakesh CB. Non-syndromic form of bilateral bimaxillary bull teeth – a case report with challenges in pediatric dentistry. OHDM. 2015;14:405–8.
Wang X, Wang J, Liu Y, Yuan B, Ruest LB, Feng JQ, Qin C. The specific role of FAM20C in dentinogenesis. J Dent Res. 2014;94(7):330–6. https://doi.org/10.1177/0022034514563334.
Whitt J, Rokos JW, Dunlap CL, Barker BF. Segmental odontomaxillary dysplasia: report of a series of 5 cases with long-term follow-up. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011;112:e29–47.
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Aps, J. (2019). Common Dental Anomalies in Pediatric Dental Practice. In: Imaging in Pediatric Dental Practice . Springer, Cham. https://doi.org/10.1007/978-3-030-12354-3_7
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DOI: https://doi.org/10.1007/978-3-030-12354-3_7
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