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Dentinogenesis Imperfecta

Known as: Dentinogenesis Imperfecta [Disease/Finding], Imperfecta, Dentinogenesis 
An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops… 
National Institutes of Health

Related topics

Related topics

16 relations
Cortical Defects, Wormian Bones, and Dentinogenesis ImperfectaDentin DysplasiaDentinogenesis imperfecta without osteogenesis imperfectaEhlers-Danlos syndrome 6B

Narrower (2)

Dentinogenesis imperfecta - Shield's type III (disorder)Hereditary Opalescent Dentin (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Dentinogenesis Imperfecta Type II–A Case Report with Review of Literature
Dentinogenesis imperfecta is a developmental disorder affecting the structure of the teeth.Both deciduous and permanent dentition… 
2014
2014
Dentinogenesis imperfecta: a case report of comprehensive treatment for a teenager.
Improving a smile can change a person's self-image. This case report describes treatment for an adolescent boy with… 
2011
2011
PROSTHODONTIC REHABILITATION OF A PATIENT WITH DENTINOGENESIS IMPERFECTA
Dentinogenesis Imperfecta is an autosomal dominant disorder of tooth development characterized by the presence of opalescent… 
2008
2008
Dentinogenesis imperfecta : a challenge for root canal treatment-case report
Dentinogenesis imperfecta (DI) is a hereditary disorder affecting both the deciduous and permanent dentition. Partially or… 
2004
2004
Amelogenesis Imperfecta in a New Animal Model—a Mutation in Chromosome 5 (human 4q21)
Candidate genes for amelogenesis imperfecta (AI) and dentinogenesis imperfecta (DI) are located on 4q21 in humans. We tested our… 
1989
1989
A Polish variant of isolated dentinogenesis imperfecta with a generalised connective tissue defect
A case is described of four generations of a Polish family with characteristic features of dentinogenesis imperfecta, who also… 
1986
1986
Osteogenesis Imperfecta: Orthopedic Aspects
Osteogenesis imperfecta (OI) is a hereditary disorder characterized primarily by excessive bone fragility. Associated… 
1983
1983
Osteogenesis imperfecta with dentinogenesis imperfecta: a mistaken case of child abuse.
1981
1981
Thirteen-year-old boy with dentinogenesis imperfecta - pedodontic and orthodontic treatment.
Dentinogenesis imperfecta is a hereditary condition characterized by disturbance in tooth formation. The colour of the teeth vary… 
1981
1981
Treatment of dentinogenesis imperfecta in a child: report of case.
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