This article describes a new case of a rare syndrome which combines uncommon conditions, such as hypoplastic amelogenenesis imperfecta (AI), delay of permanent tooth eruption, gingival enlargement, pulpal calcifications and bilateral medullary nephrocalcinosis. The importance of syndrome diagnosis and recognition in this condition is in guiding pediatric dentist, who meets this patient group in early age, to recognize the possibility of renal anomalies in patients AI in order that affected individuals might benefit from early referral to nephrology services and hence improved prognosis
The present investigation studied dental development in 23 subjects with amelogenesis imperfecta (AI...
The purpose of this article is to highlight the rare presence of gingival calcification with Amelog...
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental...
This article describes a new case of a rare syndrome which combines uncommon conditions, such as hyp...
nephrocalcinosis Abstract – This article describes a new case of a rare syndrome which combines unco...
Aim: To analyze the prevalence and associated oral findings of nephrocalcinosis in a group of patien...
Objectives Amelogenesis imperfecta (AI) refers to a group of hereditary disorders that affect the qu...
Aim: To analyze the prevalence and associated oral findings of nephrocalcinosis in a group of patien...
Background/Aims: Amelogenesis imperfecta (AI) is due to many inherited defects of enamel formation t...
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Abstract: Amelogenesis Imperfecta is a hereditary anomaly that affects the enamel of human teeth and...
Jaypee’s Internation l Jour al of linical P diatric Dentistry, September-December 2008;1(1):25-31 Ab...
Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative...
Amelogenesis imperfecta (AI) is a heterogeneous inherited disorder that disturbs the developing enam...
Amelogenesis Imperfecta (AI) is an alteration of the structure and appearance of dental enamel of ge...
The present investigation studied dental development in 23 subjects with amelogenesis imperfecta (AI...
The purpose of this article is to highlight the rare presence of gingival calcification with Amelog...
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental...
This article describes a new case of a rare syndrome which combines uncommon conditions, such as hyp...
nephrocalcinosis Abstract – This article describes a new case of a rare syndrome which combines unco...
Aim: To analyze the prevalence and associated oral findings of nephrocalcinosis in a group of patien...
Objectives Amelogenesis imperfecta (AI) refers to a group of hereditary disorders that affect the qu...
Aim: To analyze the prevalence and associated oral findings of nephrocalcinosis in a group of patien...
Background/Aims: Amelogenesis imperfecta (AI) is due to many inherited defects of enamel formation t...
Background: The aims of this study are to present sociodemographic and familial characteristics, cli...
Abstract: Amelogenesis Imperfecta is a hereditary anomaly that affects the enamel of human teeth and...
Jaypee’s Internation l Jour al of linical P diatric Dentistry, September-December 2008;1(1):25-31 Ab...
Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative...
Amelogenesis imperfecta (AI) is a heterogeneous inherited disorder that disturbs the developing enam...
Amelogenesis Imperfecta (AI) is an alteration of the structure and appearance of dental enamel of ge...
The present investigation studied dental development in 23 subjects with amelogenesis imperfecta (AI...
The purpose of this article is to highlight the rare presence of gingival calcification with Amelog...
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental...