Volume 9, Issue 2 (spring & summer 2014)
ijpd 2014, 9(2): 73-78 |
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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://jiapd.ir/article-1-43-en.html
URL: http://jiapd.ir/article-1-43-en.html
Abstract: (7960 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
Type of Article: Research Article |
Subject:
General
Received: 2015/01/28 | Accepted: 2015/01/28 | Published: 2015/01/28
Received: 2015/01/28 | Accepted: 2015/01/28 | Published: 2015/01/28
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