Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the deciduous and permanent dentitions. It is characterized by opalescent teeth composed of irregularly formed and undemineralized dentin which obliterates pulp chamber and root canal. DI can appear as a separate disorder or with osteogenesis imperfecta (OI). The teeth with DI show a grayish-blue to brown hue with dislodged enamel, dysplastic dentine with irregular dentinal tubules and interglobular dentine, short roots and pulpal obliteration, which all may lead to rapid and extensive attrition which require adequate crown reconstruction. The aim of this study was to show a reconstruction of frontal teeth in upper jaw with direct composite veneers in...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalit...
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affect...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permane...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
ackground: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, ...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Dentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth de...
INTRODUCTION: Dentinogenesis imperfecta (DI) or hereditary opalescent dentin is an autosomal dominan...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormali...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), compri...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalit...
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affect...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permane...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
ackground: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, ...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Dentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth de...
INTRODUCTION: Dentinogenesis imperfecta (DI) or hereditary opalescent dentin is an autosomal dominan...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormali...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), compri...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalit...
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affect...