Journal title
عنوان نشریه
Journal of Dentomaxillofacial
Literature & Humanities
http://3dj.gums.ac.ir
1
admin
doi
en
jalali
1392
7
1
gregorian
2013
10
1
2
3
online
1
fulltext
en
Dentin Dysplasia Type I with Hypomature Amelogenesis Imperfecta in an 18-year-old Girl
تخصصي
Radiology
پژوهشي
Original article
<b>Introduction:</b> 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.
Dentin dysplasia ,Amelogenesis imperfecta ,Dental anomalies
34
39
http://3dj.gums.ac.ir/browse.php?a_code=A-10-1-34&slc_lang=en&sid=1
Ehsan
Azma
Yes
Department of Oral Medicine, Guilan University of Medical Sciences, Dental School, Rasht, Iran
Seyed Javad
Kia
No
Department of Oral Medicine, Guilan University of Medical Sciences, Dental School, Rasht, Iran
Somayeh
Nemati
No
Department of Maxillofacial Radiology, Guilan University of Medical Sciences, Dental Faculty, Rasht, Iran