Results 11 to 20 of about 7,940 (235)
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.
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Personalized Bonding Approach for Full‐Mouth Adhesive Rehabilitation in Dentinogenesis Imperfecta [PDF]
Clin Case RepABSTRACT Dentinogenesis imperfecta is a rare genetic disorder impacting dentin structure, with an incidence of 1 in 6000 to 1 in 8000 individuals. This condition alters the tooth's color and structure, affecting patients aesthetically, functionally, and socially.
Clark C, Kérourédan O, Massé L.
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Prevalence of dentinogenesis imperfecta in a French population
Journal of International Society of Preventive and Community Dentistry, 2017 Dentinogenesis imperfecta is a genetic disorder of the dentin occurring during the tooth development. It leads to many structural changes that can be identified clinically (brownish colored teeth, cracked enamel) and radiologically (globular crown, cervical constriction, short roots, and obliterated pulp chamber and/or root canals).
Antoine Cassia +4 more
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Dentinogenesis imperfecta in a 6-year-old male neutered Labrador retriever: Case report with atypical clinical presentation and treatment review [PDF]
Frontiers in Veterinary ScienceThis 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
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Phospholipids in Amelogenesis and Dentinogenesis
Journal of Hard Tissue Biology, 2004 Phospholipids have been identified in enamel and dentin. Before demineralization, a group of phospholipids extracted by lipid solvents was associated with cell membranes and is therefore closely related to cell growth and intracellular regulations. After demineralization, a second group of phospholipids, associated with the extracellular matrix, was ...
Michel Goldberg +2 more
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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 +3 more
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The Genes Involved in Dentinogenesis [PDF]
Organogenesis, 2022 The development and repair of dentin are strictly regulated by hundreds of genes. Abnormal dentin development is directly caused by gene mutations and dysregulation. Understanding and mastering this signal network is of great significance to the study of tooth development, tissue regeneration, aging, and repair and the treatment of dental diseases.
Shuang Chen +5 more
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Laporan Kasus: Dentinogenesis Imperfekta [PDF]
STOMATOGNATIC - Jurnal Kedokteran Gigi, 2019 Dentinogenesis imperfecta is the one of most common hereditary disorder of dentin formation, especially at histodifferentiation stage. It reported have to an incidences of 1 in 8000. Dentinogenesis imperfecta is an autosomal dominant, affecting both the formation and mineralizatin of dentin.
Evellyn Islami Abdurokhman, Fadli Ashar
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Indian Journal of Dental ResearchRehabilitation of an attrited dentition is one of the most challenging task faced by a prosthodontist which requires a systematic, phase wise approach. Hobo’s techniques and Pankey Mann Schuyler’s philosophy are widely used and documented for full mouth ...
Amina +4 more
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Blue Sclera to Brittle Bones: A Rare Case of Osteogenesis Imperfecta With Dentinogenesis Imperfecta and Nephrocalcinosis. [PDF]
J Investig Med High Impact Case RepHayat S, Mayan AR, Khan MW, Hayat QJ.
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