The morphological abnormalities of the teeth of patients affected by dentinogenesis imperfecta type 2 (DI-II) may underlie the difficulties with the clinical restoration of such teeth. We therefore performed a scanning electron microscopy (SEM) study of four permanent first mandibular molars of four DI-II patients with periapical pathosis. The teeth were prepared for SEM evaluation by standard methods. In the crown, the enamel presented a highly irregular surface with a number of cracks and crevices. In some places, only granular remains of the enamel were found, while in other parts of the crown, the enamel was absent. SEM examination revealed the structural changes responsible for the lower enamel’s hardness and resistance to attrition, a...
Dentinogenesis imperfecta type II (DI-II) is the most common dental genetic disease with reported in...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
AIM: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disease that affects both decid...
AIM: Dentinogenesis Imperfecta is a hereditary defect consisting of opalescent teeth composed of i...
Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated...
The purpose of this study was to clarify the structural and ultrastructural alterations of the ename...
Abstract BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects bo...
Heritable dentin defects form a group of diseases which exclusively affect dentin among the various ...
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...
Abstract: The morphological abnormalities of the teeth of patients affected by dentinogenesis imperf...
Dentinogenesis imperfecta (DGI) is a hereditary defect consisting of opalescent teeth composed of ir...
Purpose/Aim: The aim of this study was to explore whether dentinogenesis imperfecta (DGI)-related ab...
Aim. The aim of this study was to assess the correlation between osteogenesis imperfecta (OI) and de...
Abstract AIM: The aim of this study was to assess the correlation between osteogenesis imperfecta (...
Dentinogenesis imperfecta type II (DI-II) is the most common dental genetic disease with reported in...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
AIM: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disease that affects both decid...
AIM: Dentinogenesis Imperfecta is a hereditary defect consisting of opalescent teeth composed of i...
Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated...
The purpose of this study was to clarify the structural and ultrastructural alterations of the ename...
Abstract BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects bo...
Heritable dentin defects form a group of diseases which exclusively affect dentin among the various ...
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...
Abstract: The morphological abnormalities of the teeth of patients affected by dentinogenesis imperf...
Dentinogenesis imperfecta (DGI) is a hereditary defect consisting of opalescent teeth composed of ir...
Purpose/Aim: The aim of this study was to explore whether dentinogenesis imperfecta (DGI)-related ab...
Aim. The aim of this study was to assess the correlation between osteogenesis imperfecta (OI) and de...
Abstract AIM: The aim of this study was to assess the correlation between osteogenesis imperfecta (...
Dentinogenesis imperfecta type II (DI-II) is the most common dental genetic disease with reported in...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
AIM: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disease that affects both decid...