Frequency of imperfect amelogenesis (IA) varies in different world populations. There is no information on the frequency of this entity in Colombia. This report informs the consanguinity in 3 cases of IA, the mother 36 years old and her two children of 8 and 15 years old. The same condition was found in 4 mother's relatives. This corroborates a hereditary pattern of this condition. The initial treatment for these patients is preventive, controlling them periodically and keeping in mind the appropriate handling of oral hygiene habits. A balanced diet poor in sugar or cariogenic agents and frequent teeth fluorination are the techniques to strengthen enamel traces. Later on these patients must be rehabilitated to recover both aesthet...
Aim: This clinical report describes the oral rehabilitation of a young female patient diagnosed with...
Amelogenesis Imperfecta describes a group of structural anomalies of dental enamel whose inheritance...
The purpose of the case report was to describe the treatment of a 4(1/2)-year-old boy with amelogene...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...
Amelogenesis Imperfecta is a hereditary condition affecting dental enamel without any systemic manif...
Amelogenesis imperfecta (AI) is defined as an interruption of enamel formation due to genetic inheri...
Amelogenesis imperfecta (AI) is a heterogeneous inherited disorder that disturbs the developing enam...
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Amelogenesis imperfecta is a rare genetically determined disorder charaterized by the presence of a...
Amelogenesis imperfecta is a rare, genetically determined disorder charaterized by the presence of a...
Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause dev...
Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause dev...
International audienceBackground: Hereditary enamel defect diseases are regrouped under the name “Am...
Amelogenesis imperfecta (AI) has been defined as a group of hereditary enamel defects. It can be cha...
Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative...
Aim: This clinical report describes the oral rehabilitation of a young female patient diagnosed with...
Amelogenesis Imperfecta describes a group of structural anomalies of dental enamel whose inheritance...
The purpose of the case report was to describe the treatment of a 4(1/2)-year-old boy with amelogene...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...
Amelogenesis Imperfecta is a hereditary condition affecting dental enamel without any systemic manif...
Amelogenesis imperfecta (AI) is defined as an interruption of enamel formation due to genetic inheri...
Amelogenesis imperfecta (AI) is a heterogeneous inherited disorder that disturbs the developing enam...
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Amelogenesis imperfecta is a rare genetically determined disorder charaterized by the presence of a...
Amelogenesis imperfecta is a rare, genetically determined disorder charaterized by the presence of a...
Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause dev...
Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause dev...
International audienceBackground: Hereditary enamel defect diseases are regrouped under the name “Am...
Amelogenesis imperfecta (AI) has been defined as a group of hereditary enamel defects. It can be cha...
Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative...
Aim: This clinical report describes the oral rehabilitation of a young female patient diagnosed with...
Amelogenesis Imperfecta describes a group of structural anomalies of dental enamel whose inheritance...
The purpose of the case report was to describe the treatment of a 4(1/2)-year-old boy with amelogene...