A Case of X-Linked Hypophosphatemic Rickets with Dentin Dysplasia in Mandibular Third Molars. [PDF]
Children (Basel), 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.
Okawa R +4 more
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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 and malocclusion may be associated features.
I Hemachandrika +3 more
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A novel DSPPmutation is associated with type II dentinogenesis Imperfecta in a chinese family [PDF]
BMC Medical Genetics, 2007 Background Hereditary defects of tooth dentin are classified into two main groups: dentin dysplasia (DD) (types I and II) and dentinogenesis imperfecta (DGI) (types I, II, and III).
Xianqin Zhang +28 more
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Guided endodontic treatment of multiple teeth with dentin dysplasia: a case report. [PDF]
Head Face Med, 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 ...
Krug R +5 more
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Haploinsufficiency of Dspp Gene Causes Dentin Dysplasia Type II in Mice. [PDF]
Front Physiol, 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 ...
Shi C +9 more
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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 (Basel), 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.
Papagiannis A +5 more
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Dentin dysplasia type I-A dental disease with genetic heterogeneity. [PDF]
Oral Dis, 2019 Chen D +5 more
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Beyond the diagnosis: Unraveling <i>DSPP</i> genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta. [PDF]
Jpn Dent Sci RevThe 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
Boonyakanog A +8 more
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Rootless but Erupted Teeth: Interesting Trait of Dentin Dysplasia Type I [PDF]
Iranian Journal of Orthodontics, 2017 Introduction: Tooth eruption is a complex procedure and many theories has been proposed to describe the nature of this process. Some studies, have shown that in contrast to traditional thoughts, root development is not necessary for tooth eruption and ...
Soodeh Tahmasbi +2 more
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Dentofacial Features in Schimke Immuno-Osseous Dysplasia: From Childhood to Adolescence. [PDF]
Clin Case RepABSTRACT Schimke immune‐osseous dysplasia (SIOD) is a sporadic multi‐system disorder mainly characterized by spondyloepiphyseal dysplasia, immune insufficiency, and renal failure. Little evidence is available regarding the dentofacial features of SIOD.
Sharifinejad A +3 more
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