The purpose of this article is to highlight the rare presence of gingival calcification with Amelogenesis Imperfecta. A case is presented of a 12-year-old girl with a defect of enamel in deciduous as well as permanent dentition with moderate amount of gingival hyperplasia with no positive family history of a similar condition. On the basis of history, clinical and radiographic features a diagnosis of autosomal recessive hypoplastic amelogenesis imperfecta of rough variant was made. Histopathological examination of hyperplastic gingival tissue revealed the presence of calcified bodies. An attempt is made to determine the nature of these calcified bodies by histochemical examination. The relevant literature is reviewed
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Amelogenesis imperfecta encompasses a complicated group of conditions that demonstrate developmental...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...
The purpose of this article is to highlight the rare presence of gingival calcification with Amelog...
The purpose of this article is to highlight the rare presence of gingival calcification with Ameloge...
A 12-year-old female patient presented with diffusely enlarged fibrous gingivae, enamel hypoplasia, ...
This article describes a new case of a rare syndrome which combines uncommon conditions, such as hyp...
A 12-year-old female patient presented with diffusely enlarged fibrous gingivae, enamel hypoplasia, ...
Objectives Amelogenesis imperfecta (AI) refers to a group of hereditary disorders that affect the qu...
Observation: We present a case of a 21-year-old Pakistani female with hypoplastic amelogenesis imper...
Background/Aims: Amelogenesis imperfecta (AI) is due to many inherited defects of enamel formation t...
Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative...
WOS: 000189088200002PubMed ID: 14765635Amelogenesis imperfecta is a hereditary developmental disorde...
Jaypee’s Internation l Jour al of linical P diatric Dentistry, September-December 2008;1(1):25-31 Ab...
Abstract: Amelogenesis Imperfecta is a hereditary anomaly that affects the enamel of human teeth and...
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Amelogenesis imperfecta encompasses a complicated group of conditions that demonstrate developmental...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...
The purpose of this article is to highlight the rare presence of gingival calcification with Amelog...
The purpose of this article is to highlight the rare presence of gingival calcification with Ameloge...
A 12-year-old female patient presented with diffusely enlarged fibrous gingivae, enamel hypoplasia, ...
This article describes a new case of a rare syndrome which combines uncommon conditions, such as hyp...
A 12-year-old female patient presented with diffusely enlarged fibrous gingivae, enamel hypoplasia, ...
Objectives Amelogenesis imperfecta (AI) refers to a group of hereditary disorders that affect the qu...
Observation: We present a case of a 21-year-old Pakistani female with hypoplastic amelogenesis imper...
Background/Aims: Amelogenesis imperfecta (AI) is due to many inherited defects of enamel formation t...
Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative...
WOS: 000189088200002PubMed ID: 14765635Amelogenesis imperfecta is a hereditary developmental disorde...
Jaypee’s Internation l Jour al of linical P diatric Dentistry, September-December 2008;1(1):25-31 Ab...
Abstract: Amelogenesis Imperfecta is a hereditary anomaly that affects the enamel of human teeth and...
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Amelogenesis imperfecta encompasses a complicated group of conditions that demonstrate developmental...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...