Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permanent dentition. First described in the late 19th century, it is characterized by discolored and translucent teeth ranging from grey to brownish-blue or amber. Dentinogenesis Imperfecta, type II (DGI-2) is rare and it is a severe form of the condition. Radiographically, the crowns of the teeth are bulbous with marked cervical constrictions, and the pulp chambers become obliterated over a period of time. Sensori-neural hearing loss has also been reported in some patients. This case report presents the restorative management of DGI-2 in a 44year old clergy woman whose primary complaints were poor aesthetics and lack of social acceptance. The case ...
ackground: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, ...
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. ...
Dentinogenesis imperfecta (DGI) is an autosomal dominant disorder in which both the primary and the ...
Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permane...
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affect...
INTRODUCTION: Dentinogenesis imperfecta (DI) or hereditary opalescent dentin is an autosomal dominan...
A case of dentinogenesis imperfecta type II is described. The authors also present a brief literatur...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
AIM: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disease that affects both decid...
Aim. Dentinogenesis imperfecta (DI) is an autosomal dominant disorder of tooth development. This cl...
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...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta (OI) is a heterogeneous disorder of connective tissue that manifests mainly ...
ackground: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, ...
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. ...
Dentinogenesis imperfecta (DGI) is an autosomal dominant disorder in which both the primary and the ...
Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permane...
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affect...
INTRODUCTION: Dentinogenesis imperfecta (DI) or hereditary opalescent dentin is an autosomal dominan...
A case of dentinogenesis imperfecta type II is described. The authors also present a brief literatur...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
AIM: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disease that affects both decid...
Aim. Dentinogenesis imperfecta (DI) is an autosomal dominant disorder of tooth development. This cl...
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...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta (OI) is a heterogeneous disorder of connective tissue that manifests mainly ...
ackground: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, ...
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. ...
Dentinogenesis imperfecta (DGI) is an autosomal dominant disorder in which both the primary and the ...