Results 11 to 20 of about 2,474 (180)
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 MedWe 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
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
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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 +3 more
openaire +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 +2 more
doaj +1 more source
Indian Journal of Dental SciencesDentinogenesis 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 +2 more
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Dentinogenesis imperfecta type II dentin: nanostructural mechanics analysis. [PDF]
BMC Oral HealthJia G +10 more
europepmc +3 more sources
Journal of Indian Academy of Oral Medicine and Radiology, 2003 Osteogenesis Imperfecta is a genetic disorder affecting approximately 20,000 U.S. population with multiple fracture of the bone. The, actual literature of the number of patients suffering from Osteogenesis Impcrfecta in Indian Population is still nor ...
Prabal Pal
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Restorative Management of Dentinogenesis Imperfecta in an adult - A case report
Nigerian Dental Journal, 2020 Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permanent dentition. First described in the late 19th century, it is characterized by discolored and translucent teeth ranging from grey to brownish-blue or ...
A.O. Awotile, L.L. Enone, A. Oyapero
doaj +2 more sources