Dentinogenesis Imperfecta Type II: A Case Report with Literature Review
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Abstract
Dentinogenesis imperfecta is a dentin disorder caused by gene mutation and autosomal dominant inheritance that affects both deciduous and permanent dentitions. Clinical features include the discoloration of the crown, color ranges from amber, yellow-brown or even grayish blue. Radiographic features include bulbous crowns with constriction at the cementoenamel junction, pulp chamber and root canal obliteration, short and narrow root. The enamel is normal but often detaches from the defective dentin, resulting in dentin exposure. This increases the likelihood of tooth wear and fracture, as well as the possibility of pulp exposure, which can eventually lead to tooth loss. The aim of this report was to present a 19-year-old male patient with clinical and radiological features of dentinogenesis imperfecta type II. Additionally, we reviewed the data on dentinogenesis imperfecta type II, focusing on differential diagnosis and treatment planning to emphasize the importance of an accurate diagnosis and appropriate treatment plan for these patients.
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บทความ ข้อมูล เนื้อหา รูปภาพ ฯลฯ ที่ได้รับการลงตีพิมพ์ในวิทยาสารทันตแพทยศาสตร์ มหาวิทยาลัยขอนแก่นถือเป็นลิขสิทธิ์เฉพาะของคณะทันตแพทยศาสตร์ มหาวิทยาลัยขอนแก่น หากบุคคลหรือหน่วยงานใดต้องการนำทั้งหมดหรือส่วนหนึ่งส่วนใดไปเผยแพร่ต่อหรือเพื่อกระทำการใด ๆ จะต้องได้รับอนุญาตเป็นลายลักษณ์อักษร จากคณะทันตแพทยศาสตร์ มหาวิทยาลัยขอนแก่นก่อนเท่านั้น
References
Shields ED, Bixler D, El-Kafrawy AM. A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol. 1973;18(4):543-53.
Gallusi G, Libonati A, Campanella V. SEM-morphology in dentinogenesis imperfecta type II: microscopic anatomy and efficacy of a dentine bonding system. Eur J Paediatr Dent.2006;7(1):9-17.
Fan F, Li N, Huang S, Ma J. A multidisciplinary approach to the functional and esthetic rehabi litation of dentinogenesis imperfecta type II: A clinical report. J Prosthet Dent.2019;122(2): 95-103.
Witkop CJ, Rao S. Inherited Defects in Tooth Structure. Birth Defects Orig Artic Ser.1971;7(7): :153-84.
Barron MJ, McDonnell ST, Makie I, Dixon MJ. Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia. Orphanet J Rare Dis. 2008;3:31.
Majorana A, Bardellini E, Brunelli PC, Lacaita M, Cazzolla AP, Favia G. Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study. Int J Paediatr Dent. 2010;20(2):112-8.
Syriac G, Joseph E, Rupesh S, Mathew J. Complete overlay denture for pedodontic patient with severe dentinogenesis Imperfecta. Int J Clin Pediatr Dent. 2017;10(4):394- 8.
Kim JW, Simmer JP. Hereditary dentin defects. J Dent Res. 2007;86(5):392-9.
Witkop CJ Jr. Hereditary defects of dentin. Dent Clin North Am. 1975;19(1):25-45.
Schwartz S, Tsipouras P. Oral findings in osteogenesis imperfecta. Oral Surg Oral Med Oral Pathol. 1984;57(2):161-7.
Andersson K, Malmgren B, Åström E, Dahllöf G. Dentinogenesis imperfecta type II in Swedish children and adolescents. Orphanet J Rare Dis. 2018;13(1):145.
Wieczorek A, Loster J, Ryniewicz W, Ryniewicz AM. Dentinogenesis imperfecta-hardness and Young's modulus of teeth. Acta Bioeng Biomech. 2013;15(3):65-9.
White SC, Pharoach MJ. Oral radiology: principle and interpretation. 7th ed. St. Louis:Elsevier; 2014.596.
Wieczorek A, Loster J. Dentinogenesis imperfecta type II: ultrastructure of teeth in sagittal sections. Folia Histochem Cytobiol. 2013;51(3): 244–7.
Davis GR, Fearne JM, Sabel N, Norén JG. Microscopic study of dental hard tissues in primary teeth with Dentinogenesis Imperfecta Type II: Correlation of 3D imaging using X-ray microtomography and polarising microscopy. Arch Oral Biol. 2015;60(7):1013-20.
O’Connell AC, Marini JC. Evaluation of oral problems in an osteogenesis imperfecta population. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999;87(2):189-96.
Biria M, Abbas FM, Mozaffar S, Ahmadi R. Dentinogenesis imperfecta associated with osteogenesis imperfecta. Dental Res J. 2012;9(4): 489-94.
Kerebel B, Daculsi G, Menanteau J, Kerebel LM. The inorganic phase in dentinogenesis imperfecta. J Dent Res. 1981;60:1655-60.
Tsoukala E, Chochtoula G, Theodorou I, Lambrou GI. Dentinogenesis imperfecta: An update. J Res Pract Musculoskeletal Syst. 2022;6(1):9-13.
Monteiro J, Balmer R, Lafferty F, Lyne A, Mighell A, O'Donnell K, et al. Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience. Eur Arch Paediatr Dent. 2024; 25(1):85-91.
Sánchez AR, Rogers RS 3rd, Sheridan PJ. Tetracycline and other tetracycline-derivative staining of the teeth and oral cavity. Int J Dermatol. 2004;43(10):709-15.
Vennila V, Madhu V, Rajesh R, Ealla KKR, Velidandla SR, Santoshi S. Tetracycline-induced discoloration of deciduous teeth: case series. J Int Oral Health. 2014;6(3):115-9.
Desjardins MP, Naccache L, Hébert A, Auger I, Teira P, Pelland-Marcotte MC. Very early diagnosis and management of congenital erythropoietic porphyria. Clin Pediatr (Phila). 2023;62(5):399-403.
Fayle SA, Pollard MA. Congenital erythropoietic porphyria- oral manifestations and dental treatment in childhood: a case report. Quintessence Int 1994;25(8):551-4.
Okawa R, Nakano K. Dental manifestation and management of hypophosphatasia. Jpn Dent Sci Rev. 2022;58:208-16.
Su T, Zhu Y, Wang X, Zhu Q, Duan X. Hereditary dentin defects with systemic diseases. Oral Dis. 2023;29(6):2376-93.
Garrocho-Rangel A, Dávila-Zapata I, Martínez-Rider R, Ruiz-Rodríguez, Pozos-Guillén A. dentinogenesis imperfecta type II in children: A scoping review. J Clin Pediatr Dent. 2019;43(3):147-54.
Sapir S, Shapira J. Dentinogenesis imperfecta: An early treatment strategy. Pediatr Dent. 2001;23(3): 232–7.
Stewart RE, Luke LS, Pike AR. Preformed polycarbonate crowns for the restoration of anterior teeth. J Am Dent Assoc. 1974;88(1):103–7.
Darendeliler-Kaba A, Marechaux SC. Hereditary dentinogenesis imperfecta: a treatment program using an overdenture. ASDC J Dent Child. 1992;59(4):273-6.
Kaur R, Karadwal A, Sharma D, Sandhu MK. Dentinogenesis imperfecta type II: Diagnosis, functional and esthetic rehabilitation in mixed dentition. J Oral Maxillofac Pathol.2021;25(Suppl 1):S76-S80.
Soliman S, Meyer-Marcotty P, Hahn B, Halbleib K, Krastl G. Treatment of an adolescent patient with dentinogenesis imperfecta using indirect composite restorations-A case report and literature review. J Adhes Dent. 2018;20(4):345-54.
Lygidakis NA, Smith R, Oulis CJ. Scanning electron microscopy of teeth in osteogenesis imperfecta type I. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1996;81:567-72.
Witkop CJ, Rao S. Inherited defects in tooth structure. Birth Defects Orig Artic Ser.1971;7(7): 153-84.
Teixeira CS, Felippe MCS, Felippe WT, Silva-Sousa YTC, Sousa-Neto MD. The role of dentists in diagnosing osteogenesis imperfecta in patients with dentinogenesis imperfecta. J Am Dent Assoc. 2008;139(7):906-14.
