Volume 2, Issue 3 (10-2013)
2013, 2(3): 34-39 |
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1- Department of Oral Medicine, Guilan University of Medical Sciences, Dental School, Rasht, Iran
2- Department of Maxillofacial Radiology, Guilan University of Medical Sciences, Dental Faculty, Rasht, Iran
2- Department of Maxillofacial Radiology, Guilan University of Medical Sciences, Dental Faculty, Rasht, Iran
Abstract: (10767 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.
Type of Study: Original article |
Subject:
Radiology
Received: 2013/12/30 | Accepted: 2013/12/30 | Published: 2013/12/30
Received: 2013/12/30 | Accepted: 2013/12/30 | Published: 2013/12/30
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