چکیده: (10744 مشاهده)
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.
نوع مطالعه:
پژوهشي |
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تخصصي دریافت: 1392/10/9 | پذیرش: 1392/10/9 | انتشار: 1392/10/9