Literature DB >> 23102800

Cleidocranial dysplasia: a review of the dental, historical, and practical implications with an overview of the South African experience.

Tina Roberts1, Lawrence Stephen, Peter Beighton.   

Abstract

Cleidocranial dysplasia (CCD) is an uncommon but well-known genetic skeletal condition. Several hundred affected persons are members of a large extended family in the Cape Town Mixed Ancestry community of South Africa. The clinical manifestations are often innocuous, but hyperdontia and other developmental abnormalities of the teeth are a major feature and may require special dental management. Over the past 40 years, the authors have encountered more than 100 affected persons in Cape Town. Emphasis has been on dental management, but medical, genetic, and social problems have also been addressed. In this article, we have reviewed the manifestations of the disorder in the light of our own experience, and performed a literature search with emphasis on the various approaches to dental management and treatment options in CCD. Advances in the understanding of the biomolecular pathogenesis of CCD are outlined and the international and local history of the disorder is documented.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 23102800     DOI: 10.1016/j.oooo.2012.07.435

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol


  21 in total

1.  Cleidocranial dysplasia: complete clinical, radiological and histological profiles.

Authors:  Ruchieka Vij; Puneet Batra; Hitesh Vij
Journal:  BMJ Case Rep       Date:  2013-03-20

2.  Surgical Management and Evaluation of the Craniofacial Growth and Morphology in Cleidocranial Dysplasia.

Authors:  Stephen L Greene; Chung How Kau; Somsak Sittitavornwong; Kathlyn Powell; Noel K Childers; Mary MacDougall; Ejvis Lamani
Journal:  J Craniofac Surg       Date:  2018-06       Impact factor: 1.046

3.  Classical cleidocranial dysplasia in an adult, due to a novel frameshift pathogenic variant in RUNX2.

Authors:  Malavika Hebbar; Katta M Girisha; Anju Shukla
Journal:  BMJ Case Rep       Date:  2016-05-13

4.  Appropriateness of standard cephalometric norms for the assessment of dentofacial characteristics in patients with cleidocranial dysplasia.

Authors:  Fabio Savoldi; Francesca Del Re; Ingrid Tonni; Min Gu; Domenico Dalessandri; Luca Visconti
Journal:  Dentomaxillofac Radiol       Date:  2021-11-17       Impact factor: 2.419

5.  Histological examination and clinical evaluation of the jawbone of an adult patient with cleidocranial dysplasia: a case report.

Authors:  Sigmar Schnutenhaus; Ralph G Luthardt; Heike Rudolph; Werner Götz
Journal:  Int J Clin Exp Pathol       Date:  2015-07-01

6.  Multiple unerupted and supernumerary teeth in a patient with cleidocranial dysplasia.

Authors:  Galal Omami
Journal:  Radiol Case Rep       Date:  2017-12-07

7.  Periodontal ligament stem cells modulate root resorption of human primary teeth via Runx2 regulating RANKL/OPG system.

Authors:  Bei Li; Yu Zhang; Qingchao Wang; Zhiwei Dong; Linjuan Shang; Lizheng Wu; Xiaojing Wang; Yan Jin
Journal:  Stem Cells Dev       Date:  2014-06-26       Impact factor: 3.272

8.  Orthodontic and surgical management of cleidocranial dysplasia.

Authors:  Tina Keun Nan Park; Karin Vargervik; Snehlata Oberoi
Journal:  Korean J Orthod       Date:  2013-10-25       Impact factor: 1.372

9.  Cleidocranial dysplasia syndrome (CCD) with an unusual finding in a young patient.

Authors:  Parul Singhal; Anita Singhal; Cheranjeevi Jayam; Anila Bandlapalli
Journal:  BMJ Case Rep       Date:  2015-11-18

Review 10.  A review of clinical and radiological features of cleidocranial dysplasia with a report of two cases and a dental treatment protocol.

Authors:  S Arun Paul; S Sibu Simon; A Kaneesh Karthik; Rabin K Chacko; S Savitha
Journal:  J Pharm Bioallied Sci       Date:  2015-08
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.