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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
Full-Text [PDF 528 kb]   (683 Downloads)    
Type of Article: Research | Subject: General
Received: 2015/01/28 | Accepted: 2015/01/28 | Published: 2015/01/28
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References
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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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