Literature DB >> 29895546

Dentin dysplasia: diagnostic challenges.

Ahmed Alhilou1, Hannah P Beddis1, Alan J Mighell2, Kathryn Durey1.   

Abstract

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. Clinical signs include spontaneous abscess formation or increased tooth mobility which can lead to exfoliation. DD can therefore have a significant impact on the patient's dentition, and treatment is often challenging. Shields' classification of dentin disorders has been recently criticised for failing to consider differential variations and expressions of these disorders. This paper describes a case of a 23-year-old woman with previously undiagnosed DD, who presented with clinical and histological features belonging to several of these diseases, thus highlighting the potential diagnostic challenges faced with Shields' classification. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  dentistry and oral medicine; genetics

Mesh:

Year:  2018        PMID: 29895546      PMCID: PMC6011466          DOI: 10.1136/bcr-2017-223942

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  18 in total

1.  A splicing mutation in VPS4B causes dentin dysplasia I.

Authors:  Qi Yang; Dong Chen; Fu Xiong; Danna Chen; Cuixian Liu; Yanhui Liu; Qiuxia Yu; Jun Xiong; Jinzhong Liu; Kunyang Li; Lingfeng Zhao; Yuhua Ye; Hong Zhou; Lingling Hu; Zhihui Tian; Xuan Shang; Leitao Zhang; Xiaofeng Wei; Wanjun Zhou; Dongri Li; Wenqing Zhang; Xiangmin Xu
Journal:  J Med Genet       Date:  2016-05-31       Impact factor: 6.318

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Journal:  J Endod       Date:  1979-12       Impact factor: 4.171

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Journal:  Oral Surg Oral Med Oral Pathol       Date:  1994-09

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Journal:  Br J Oral Maxillofac Surg       Date:  1984-08       Impact factor: 1.651

Review 5.  Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.

Authors:  Muriel de La Dure-Molla; Benjamin Philippe Fournier; Ariane Berdal
Journal:  Eur J Hum Genet       Date:  2014-08-13       Impact factor: 4.246

6.  Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects.

Authors:  Agnès Bloch-Zupan; Xavier Jamet; Christelle Etard; Virginie Laugel; Jean Muller; Véronique Geoffroy; Jean-Pierre Strauss; Valérie Pelletier; Vincent Marion; Olivier Poch; Uwe Strahle; Corinne Stoetzel; Hélène Dollfus
Journal:  Am J Hum Genet       Date:  2011-12-09       Impact factor: 11.025

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Authors:  Shohreh Ravanshad; Akbar Khayat
Journal:  Aust Endod J       Date:  2006-04       Impact factor: 1.659

Review 8.  Hereditary dentin defects.

Authors:  J-W Kim; J P Simmer
Journal:  J Dent Res       Date:  2007-05       Impact factor: 6.116

9.  Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.

Authors:  Fu Xiong; Zhisong Ji; Yanhui Liu; Yu Zhang; Lingling Hu; Qi Yang; Qinwei Qiu; Lingfeng Zhao; Dong Chen; Zhihui Tian; Xuan Shang; Leitao Zhang; Xiaofeng Wei; Cuixian Liu; Qiuxia Yu; Meichao Zhang; Jing Cheng; Jun Xiong; Dongri Li; Xiuhua Wu; Huijun Yuan; Wenqing Zhang; Xiangmin Xu
Journal:  Hum Mutat       Date:  2016-10-19       Impact factor: 4.878

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Authors:  R K Wesley; G P Wysoki; S M Mintz; J Jackson
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1976-04
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  1 in total

1.  Guided endodontic treatment of multiple teeth with dentin dysplasia: a case report.

Authors:  Ralf Krug; Julian Volland; Sebastian Reich; Sebastian Soliman; Thomas Connert; Gabriel Krastl
Journal:  Head Face Med       Date:  2020-11-17       Impact factor: 2.246

  1 in total

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