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:: Volume 9, Issue 2 (spring & summer 2014) ::
ijpd 2014, 9(2): 73-78 Back to browse issues page
Dentinogenesis Imperfecta type II: A case report
P Moini Dr , M Afsharianzadeh Dr, E Abdoli Tafti Dr
Abstract:   (5065 Views)
Dentinogenesis Imperfecta type II or hereditary opalescent dentin is inherited as an autosomal dominant trait, that affects both primary and permanent dentition. It occurs in both sex. Clinically, this disorder is characterized by yellowish brown teeth with structural defects such as bulbous crown and small pulp chambers, radiographically. The underlying defect of mineralization often results in shearing of the overlying enamel leaving exposed weakened dentin which is prone to wear. In this article, a 6 year old Iranian boy with Dentinogenesis Imperfecta and his recommended treatment plan is reported.
Keywords: Dentinogenesis Imperfecta
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Type of Article: Research | Subject: General
Received: 2015/01/28 | Accepted: 2015/01/28 | Published: 2015/01/28
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1. Shetty N, Joseph M, Basnet P, Dixit S. An integrated treatment approach: a case report for dentinogenesis imperfecta type II. Kathmandu Univ Med J. 2007; 5(2):230-3.
2. Barron MJ, Mcdonnell ST, Mackie I, Dixon MJ. Hereditary dentin disorders: dentinogenesis imperfecta and dentin dysplasia. Orphanet J Rare Dis. 2008; 3:31. [DOI:10.1186/1750-1172-3-31]
3. Pinkham J, Casamassimo P, MCTigue D, Fields H. Pediatric dentistry: Infancy through adolescence.4th Ed. Philadelphia: Elseviers Saunders; 2005.
4. Mott D, Patel M, Park DC. Dental rehabilitation of a patient with dentinogenesis imperfecta: a clinical report. The army medical department journal. 2011:95-7.
5. Kamboj M, Chandra A. Dentinogenesis imperfecta type II: an affected family saga. J Oral Sci. 2007; 49(3):241-4. [DOI:10.2334/josnusd.49.241]
6. Tsai CL, Lin YT, Lin YT. Dentinogenesis imperfecta associated with Osteogenesis imperfecta: report of two cases. Chang Gung Med J. 2003; 26:138-43.
7. Delgado AC, Ruiz M, Alarcon JA, Gonzalez E. Dentinogenesis imperfecta: the importance of early treatment. Quintessence Int. 2008; 39(3):257-63.
8. Goud A, Deshpande S. Prosthodontic rehabilitation of dentinogenesis imperfecta. Contemp Clin Dent. 2011; 2(2):138-41. [DOI:10.4103/0976-237X.83072]
9. Gupta S, Bhowate R, Bhati A. Hereditary opalescent dentin: a report of two cases. J Contemp Dent Pract. 2010; 11(4):1-5.
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Moini P, Afsharianzadeh M, Abdoli Tafti E. Dentinogenesis Imperfecta type II: A case report. ijpd. 2014; 9 (2) :73-78
URL: http://journal.iapd.ir/article-1-43-en.html

Volume 9, Issue 2 (spring & summer 2014) Back to browse issues page
مجله دندانپزشکی کودکان ایران Iranian Journal of Pediatric Dentistry
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