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Dentinogenesis imperfecta (DI) is a genetic disorder of tooth development. It is inherited in an autosomal dominant pattern, as a result of mutations on chromosome 4q21, in the dentine sialophosphoprotein gene (DSPP). It is one of the most frequently occurring autosomal dominant features in humans. Dentinogenesis imperfecta affects an estimated 1 in…
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teeth dentin dentinogenesis imperfecta type may tooth dental di condition pulp attrition enamel permanent associated roots primary classification clinical due
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Dentinogenesis imperfecta | Specialty | Dentistry | 1.00 | infobox |
| tooth decay | instance of | or total pulp obliterationSmall or obliterated root canalPresence of pulp stonesNarrow and small rootsPeriapical radiolucency without any evidence of clinical pathology | 0.80 | text |
| tetracyclines | instance of | Papillon-Lefevre syndromePermanent tooth discolouration caused by medications | 0.80 | text |
| or medical conditions such as rickets Differential diagnosisHypocalcified forms of amelogenesis imperfectaCongenital erythropoietic porphyriaConditions that can cause early loss of teeth e.g | instance of | Papillon-Lefevre syndromePermanent tooth discolouration caused by medications | 0.80 | text |
| or medical conditions such as rickets TreatmentPreventive | instance of | Papillon-Lefevre syndromePermanent tooth discolouration caused by medications | 0.80 | text |
| restorative care are important as well as aesthetics as a consideration | instance of | Papillon-Lefevre syndromePermanent tooth discolouration caused by medications | 0.80 | text |
| orthodontics | instance of | many common cosmetic procedures | 0.80 | text |
| extractions.Dental professionals should therefore proceed with caution when carrying out any dental procedures in patients who have Type 1 DI who may be on bisphosphonate drug therapy | instance of | Occurrences of this risk is associated with dental surgical procedures | 0.80 | text |
| Dentinogenesis imperfecta | related to de La Dure-Molla, Foruner and Berdal (2015) | La Dure-Molla | 0.60 | section |
| Dentinogenesis imperfecta | related to de La Dure-Molla, Foruner and Berdal (2015) | Foruner | 0.60 | section |
| Dentinogenesis imperfecta | related to de La Dure-Molla, Foruner and Berdal (2015) | Berdal | 0.60 | section |
| Dentinogenesis imperfecta | related to de La Dure-Molla, Foruner and Berdal (2015) | Shield Classification | 0.60 | section |
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