Literature DB >> 1554531

Dental treatment strategies in cleidocranial dysplasia.

B L Jensen1, S Kreiborg.   

Abstract

Based on the findings of our recent longitudinal study on the abnormalities of the dentition in cleidocranial dysplasia (CCD), a hypothesis has been proposed, which makes it possible to predict time of onset of formation of supernumerary teeth and their location in the jaws. It was found that a diagnosis should be made early so that formation of supernumerary teeth can be diagnosed and early intervention undertaken. It should be possible to diagnose supernumerary incisors at about 5-7 years of age and supernumerary canines and premolars a few years later. When root length of the normal permanent teeth has reached about one third of its final length, the overlying supernumerary teeth should be removed, together with overlying bone and primary teeth. In regions where no supernumerary teeth are formed, eruption may also be improved by removal of the primary teeth and surgical exposure of the underlying permanent teeth. Conventional orthodontic treatment and eventually autotransplantation of teeth may still be necessary in the future, but it can be anticipated that the new strategy, with much earlier intervention, will materially reduce the extent of surgical and orthodontic interventions, which have previously been of extremely long duration, tedious to the patients and often of limited success.

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Mesh:

Year:  1992        PMID: 1554531     DOI: 10.1038/sj.bdj.4807836

Source DB:  PubMed          Journal:  Br Dent J        ISSN: 0007-0610            Impact factor:   1.626


  17 in total

1.  Dental treatment strategies in a 40-year-old patient with cleidocranial dysplasia.

Authors:  Aneta Olszewska
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

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

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

3.  Clinical and Radiological Evaluation of Cleidocranial Dysplasia in Two Trinidadian Siblings.

Authors:  A K Bissoon; K Moze
Journal:  West Indian Med J       Date:  2014-07-22       Impact factor: 0.171

Review 4.  Cleidocranial dysplasia: clinical and molecular genetics.

Authors:  S Mundlos
Journal:  J Med Genet       Date:  1999-03       Impact factor: 6.318

5.  Characterization of dental phenotype in patients with cleidocranial dysplasia using longitudinal data.

Authors:  Sang-Woon Ha; Yu-Jin Jung; Han-Sol Bae; Hyun-Mo Ryoo; Il-Sik Cho; Seung-Hak Baek
Journal:  Angle Orthod       Date:  2018-04-17       Impact factor: 2.079

6.  Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia.

Authors:  C Bergwitz; A Prochnau; B Mayr; F J Kramer; M Rittierodt; H L Berten; J E Hausamen; G Brabant
Journal:  J Inherit Metab Dis       Date:  2001-11       Impact factor: 4.982

7.  Cleidocranial dysplasia: A report of two cases with brief review.

Authors:  Kusum Bharti; Mridula Goswami
Journal:  Intractable Rare Dis Res       Date:  2016-05

8.  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

9.  Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.

Authors:  Taketoshi Yoshida; Hirokazu Kanegane; Motomi Osato; Masatoshi Yanagida; Toshio Miyawaki; Yoshiaki Ito; Katsuya Shigesada
Journal:  Am J Hum Genet       Date:  2002-08-26       Impact factor: 11.025

10.  Scheuthauer-Marie-Sainton syndrome.

Authors:  Vikas Elias Kuruvila; N Bilahari; George Attokkaran; Beena Kumari
Journal:  Contemp Clin Dent       Date:  2012-07
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