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n. dentinogénesis, formación de la dentina.
References in periodicals archive ?
Joe was born with Dentinogenesis Imperfecta, a genetic defect that has affected him physically and emotionally.
When a tooth injury, dental pulp is involved in reparative dentinogenesis and deposits a new dentin matrix to repair the injured site (Renjen et al.
However, the genes regulating enamel and dentine formation are highly specific for teeth, and their mutations are associated with dental disorders such as amelogenesis imperfecta, dentinogenesis imperfecta, dentine dysplasia and isolated anomalies of tooth number and size [Bailleul-Forestier et al.
They describe a 19-year-old Soldier's presentation with a condition known as dentinogenesis imperfecta, a genetic disorder that affects the majority of the teeth, which, without treatment, ultimately results in serious deterioration and tooth loss.
Three patients (2 with obvious dentinogenesis imperfecta) had normal-colored sclerae (type IV).
Dentinogenesis Imperfecta Synonyms such as hereditary opalescent dentin have been used to describe opalescent brown teeth as a heritable, isolated defect.
This e-book covers research on these specific proteins, including details about the cells producing these molecules, their impact on bone and teeth pathology (osteogenesis and dentinogenesis imperfecta) and the potential of these molecules in promoting of inhibiting mineralization.
Changes in dental enamel such as amelogenesis imperfecta, dentinogenesis imperfecta, hypoplasia, diffuse opacities, white spot lesions, tetracycline staining, erosion, fluorosis, white cuspal and marginal ridges were excluded from the study.
Dentinogenesis imperfecta (DGI) is defined as an autosomal dominant disorder in dentin mineralization in both the primary and permanent dentitions.
Some people with OI have brittle, discolored teeth, a condition known as dentinogenesis imperfecta.
The processing of DMP1 is crucial in osteogenesis and dentinogenesis, and a failure in this processing would cause defective mineralisation in bone and dentine, as observed in X-linked hypophosphatemic rickets.
Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification.