Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult to diagnose in its mild form. The authors describe a clinical case of a diagnosis of dentinogenesis imperfecta (DI), In which a literature review combined with an analysis of dental alterations led to indications of OI involvement. Case Description. Since DI can be associated with OI, the authors reviewed correlated studies and obtained a new medical history from the patient. They then conducted a radiographic and clinical examination of the dentition and submitted an affected third molar to scanning electron microscopy analysis. They compared their findings with descriptions of OI type I dental alterations in the literature and confirmed thei...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Abstract Background Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mu...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Aim. The aim of this study was to assess the correlation between osteogenesis imperfecta (OI) and de...
This paper presents a review of dentinogenesis imperfecta occurring in patients with osteogenesis im...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Abstract AIM: The aim of this study was to assess the correlation between osteogenesis imperfecta (...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis Imperfecta is a genetic disorder affecting approximately 20,000 U.S. population with mu...
Abstract Background To report on dental characteristics and treatment load in Danish adult patients ...
Abstract BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects bo...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Abstract Background Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mu...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Aim. The aim of this study was to assess the correlation between osteogenesis imperfecta (OI) and de...
This paper presents a review of dentinogenesis imperfecta occurring in patients with osteogenesis im...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Abstract AIM: The aim of this study was to assess the correlation between osteogenesis imperfecta (...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis Imperfecta is a genetic disorder affecting approximately 20,000 U.S. population with mu...
Abstract Background To report on dental characteristics and treatment load in Danish adult patients ...
Abstract BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects bo...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Abstract Background Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mu...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...