Results 1 to 10 of about 2,152 (168)
Rootless teeth: Dentin dysplasia type I
Contemporary Clinical Dentistry, 2013 A rare case of hereditary disturbance of dentine, Dentin dysplasia type I is presented, which is characterized by short or total absence of roots, obliterated pulp chambers, and peri-apical radiolucencies. It affects both primary and secondary dentition.
Sangamesh G Fulari, Deepti P Tambake
doaj +4 more sources
A Case of X-Linked Hypophosphatemic Rickets with Dentin Dysplasia in Mandibular Third Molars [PDF]
Children, 2022 X-linked hypophosphatemic rickets (XLH) is a disease characterized by impaired bone mineralization, and its dental features include gingival abscesses and large pulp spaces due to dentin dysplasia.
Rena Okawa +4 more
doaj +2 more sources
Guided endodontic treatment of multiple teeth with dentin dysplasia: a case report [PDF]
Head & Face Medicine, 2020 Background To report the outcome of guided endodontic treatment (GET) of a case of dentin dysplasia with pulp canal calcification (PCC) and apical periodontitis based on the use of a 3D-printed template designed by merging cone-beam computed tomography ...
Ralf Krug +5 more
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Haploinsufficiency of Dspp Gene Causes Dentin Dysplasia Type II in Mice [PDF]
Frontiers in Physiology, 2020 Dentin dysplasia (DD) and dentinogenesis imperfecta (DGI) patients have abnormal structure, morphology, and function of dentin. DD-II, DGI-II, and DGI-III are caused by heterozygous mutations in the dentin sialophosphoprotein (DSPP) gene in humans ...
Ce Shi +17 more
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Dentin dysplasia: diagnostic challenges. [PDF]
BMJ Case Rep, 2018 Dentin dysplasia(DD) is a rare autosomal dominant disorder associated with disturbance of the dentin. While the crowns appear clinically normal, on radiography, the pulp spaces appear partially or completely obliterated, with short blunted roots, and multiple periapical radiolucencies affecting the apparently sound teeth.
Alhilou A +3 more
europepmc +4 more sources
Orthodontic Treatment of a Patient with Dentin Dysplasia Type I and Bilateral Maxillary Canine Impaction: Case Presentation and a Family-Based Genetic Analysis [PDF]
Children, 2021 Dentin dysplasia is a rare hereditary disorder, transmitted by autosomal dominant mode, affecting both dentin and pulp. In Type I crown morphology is normal, but root dentin organization loss leads to shorter roots.
Alexandros Papagiannis +5 more
doaj +2 more sources
Dentin dysplasia type I. [PDF]
BMJ Case Rep, 2013 Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterised clinically by nearly normal appearing crowns and hypermobility of teeth that affects one in every 100 000 individuals and manifests in both primary and permanent dentitions.
Singh A, Gupta S, Yuwanati MB, Mhaske S.
europepmc +4 more sources
Radicular dentin dysplasia: A case report
Journal of Dr. NTR University of Health Sciences, 2015 Dentin dysplasias form a rare group of hereditary dentin malformations characterized clinically by normal appearing crowns but extreme mobility of teeth due to defective root formation. Both deciduous and permanent teeth may be affected. Delayed eruption
I Hemachandrika +3 more
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Beyond the diagnosis: Unraveling DSPP genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta [PDF]
Japanese Dental Science ReviewThe DSPP gene regulates dentin mineralisation, and its pathogenic variants cause a spectrum of defects ranging from dentin dysplasia (DD-II) to dentinogenesis imperfecta (DGI-II/III). Clinical variability often confounds diagnosis. This systematic review
Angkana Boonyakanog +8 more
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Journal of Dental School, 2020 Objectives Dentin dysplasia (DD) is a rare disorder, which is not accentuated in dental practice. DD has 2 types. Type I is manifested by tooth mobility, short roots, reduced pulp space and normal crowns. Type II or coronal DD is characterized by normal
Robab Noormohammadi, Zeynab Pirayesh
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