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:: Volume 2, Number 3 (10-2013) ::
3dj 2013, 2(3): 34-39 Back to browse issues page
Dentin Dysplasia Type I with Hypomature Amelogenesis Imperfecta in an 18-year-old Girl
Ehsan Azma , Seyed Javad Kia, Somayeh Nemati
Assistant Professor Department of Oral Medicine, Guilan University of Medical Sciences, Dental School, Rasht, Iran
Abstract:   (7844 Views)
Introduction: Dentin dysplasia is a rare autosomal dominant inheriting disturbance of dentin formation characterized by normal enamel formation, but atypical dentin with abnormal pulpal morphology. There are two major patterns: type I and type II. Amelogenesis imperfecta is an autosomal dominant. X-link inherent disease that is classified by clinical manifestation into hypoplastic, hypomature, hypocalcified. The simultaneous occurrence of dentin dysplasia and amelogenesis imperfecta is quite rare. The purpose of this case report is to pre-sent a case of dentin dysplasia type I which is also associated with hypoplastic amelogenesis imperfecta in an 18 year old girl, without any syndromic signs.
Keywords: Dentin dysplasia, Amelogenesis imperfecta, Dental anomalies
Full-Text [PDF 79 kb]   (434 Downloads)    
Type of Study: Original article | Subject: Radiology
Received: 2013/12/30 | Accepted: 2013/12/30 | Published: 2013/12/30
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DOI: 10.18869/acadpub.3dj.2.3.34


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Azma E, Kia S J, Nemati S. Dentin Dysplasia Type I with Hypomature Amelogenesis Imperfecta in an 18-year-old Girl. 3dj. 2013; 2 (3) :34-39
URL: http://3dj.gums.ac.ir/article-1-58-en.html
Volume 2, Number 3 (10-2013) Back to browse issues page
مجله دانشکده دندانپزشکی دانشگاه علوم پزشکی گیلان Journal of Dentomaxillofacial
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