This case report details the diagnosis and treatment of dentinogenesis imperfecta in a 6-year-old neutered male Labrador, presenting without concurrent osteogenesis imperfecta.
Karolina Maria Piekos +4 more
doaj +1 more source
Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report
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 +2 more
doaj
Dentin Autograft as a Pulp Capping Material: A Systematic Review. [PDF]
Chaudhari WA +5 more
europepmc +1 more source
A radiological case series of three siblings with osteogenesis imperfecta and shared paternal inheritance. [PDF]
Nelwan DA +4 more
europepmc +1 more source
Beyond the diagnosis: Unraveling <i>DSPP</i> genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta. [PDF]
Boonyakanog A +8 more
europepmc +1 more source
Functional and Aesthetic Treatment of Patients With Tooth Structure Anomalies: A Narrative Review. [PDF]
Reuter AK, Ehlers V.
europepmc +1 more source
Rare spontaneous formation of a dentin bridge post-dental trauma: A cone beam computed tomography-based case report with root canal therapy. [PDF]
Rostami M +3 more
europepmc +1 more source
New Immunohistochemical Findings on Amelogenin and Dentin Sialophosphoprotein in Genetic Tooth Diseases. [PDF]
Camacho-Escalera C +4 more
europepmc +1 more source
A Novel DSPP Mutation in Dentinogenesis Imperfecta Shields Type II: Clinical, Genetic and Stem Cell Perspectives. [PDF]
Gao Q +5 more
europepmc +1 more source

