Results 11 to 20 of about 4,451 (219)

Clinical manifestations and dental management of dentinogenesis imperfecta associated with osteogenesis imperfecta: Case report

Saudi Dental Journal, 2013
Dentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic disorder that affects the connective tissues and results in dentine dysplasia.
Halima Abukabbos, Faisal Al-Sineedi
doaj   +2 more sources

A Novel Variant in Dentin Sialophosphoprotein (DSPP) Gene Causes Dentinogenesis Imperfecta Type III: Case Report. [PDF]

Mol Genet Genomic Med
We report a family with dentinogenesis imperfecta III. The proband and her mother showed rapid attrition and opalescent discoloration of teeth. The primary teeth showed “shell teeth” radiographically. We performed WES and Sanger sequencing on them and revealed a novel variant (c.38C>A: p.A13E) in the signal peptide region of the DSPP gene.
Wang Y, Xu X, Ding Y, Yuan G.
europepmc   +4 more sources

Nonsyndromic dentin genetic diseases: Dentinogenesis imperfecta Type III: A unique presentation of rhizomegaly, taurodontism, and dilacerated roots

Saudi Journal of Oral Sciences, 2021
Genetic disorders of the dentin are known for several years, and reviews have been published mainly in the form of case reports. Dentinogenesis imperfecta (DI) is a disease characterized by an abnormal formation and abnormal structure of the dentin ...
Vela D Desai, Rajeev Chitguppi
doaj   +2 more sources

Oral Health-Related Quality of Life in Dutch Adults With Osteogenesis Imperfecta. [PDF]

Oral Diseases, Volume 31, Issue 3, Page 983-992, March 2025.
Objective: To explore the oral health-related quality of life and its possible risk factors among adults with Osteogenesis Imperfecta using the Oral Health Impact Profile (OHIP)-49 questionnaire.
Appelman-Dijkstra, Natasha, Blokland, Lieke, de Kuijper, Maurits, de Kuijper-Timmermans, Emmanuelle, Gooijer, Koert, Harsevoort, Arjan, Janus, Guus, Kalaykova, Stanimira, Zillikens, Carola   +8 more
core   +2 more sources

Dentinogenesis imperfecta: The Genetic Causes and Outcomes [PDF]

, 2021
Dentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth development irregularities, and decreased tooth strength. This autosomal dominant disorder is identified in individuals of all ages.
Johnson, Sydney P, Ms.
core   +3 more sources

Osteogenesis Imperfecta/Lobstein Syndrome associated with Dentinogenesis Imperfecta

The Journal of Contemporary Dental Practice, 2013
ABSTRACT Osteogenesis imperfecta is a collagen related disorder characterized by increased bone fragility and low bone mass. The important oral finding in osteogenesis imperfect is the presence of dentinogenesis imperfecta. This article presents a case of osteogenesis imperfecta (type IV B) with dentinogenesis imperfecta where a 7-year-old girl had ...
Naresh, Lingaraju, P J, Nagarathna, R, Vijayalakshmi, P, Sheshadri   +3 more
openaire   +3 more sources

Dentinogenesis imperfecta type 1-Shield’s classification (1973): a rare case report and literature review [PDF]

, 2023
Dentinogenesis imperfecta (DI) is an autosomal dominant disorder that affects the dentin development. It is characterized by the presence of opalescent dentin, with dusky blue to brownish discoloration of the teeth.
Gopal, Saraswathi K., S., Priyadharshini, V., Poongodi   +2 more
core   +3 more sources

Esthetic-based Dental Management of Dentinogenesis Imperfecta in a 2.5-year-old Child [PDF]

Journal of Kerman University of Medical Sciences, 2021
Background: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, which occurs in the absence of any systemic disorder. The patients with DI presented rapid and severe attrition in primary teeth, which causes functional
Leyli Sadri, Soroush Sadri, Najmeh Akhlaghi, hamid sarlak   +3 more
doaj   +3 more sources

Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report [PDF]

Frontiers in Dentistry, 2016
Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi, Ali-Reza Eshghi, Mehrnaz Mohamadpour   +2 more
doaj   +1 more source

Dentinogenesis Imperfecta Type I and II: A Case Series Highlighting Clinical and Radiographic Insights

Indian Journal of Dental Sciences
Dentinogenesis imperfecta (DI) is a rare hereditary disorder affecting the dentin structure of both primary and permanent teeth, characterized by discoloration, structural fragility, and distinctive radiographic features.
K. Kavitha, Parikh J. Shilpa, Shah S. Jigna   +2 more
doaj   +2 more sources