Literature DB >> 29795503

32 and you - genetic testing for dental disorders.

M Harrison1,2, C-J Bushell2,3, M Irving4.   

Abstract

Genetic testing for serious illness and disease is becoming increasingly embedded in NHS healthcare. It can confirm a clinical diagnosis or guide therapy. Genetic testing for dental developmental disorders has moved beyond the realms of rarified grant-funded research groups and is now sufficiently rapid and affordable to be offered as part of a clinical service in some dental teaching hospitals. The first presentation of some genetic diseases may be in the dental surgery, so the family dentist should hone their diagnostic skills to identify patients who would benefit from referral to a genetics service. While diagnosis may sometimes guide treatment, there are now examples where it can even lead to cure. This article aims to describe some concepts and issues that a dentist should consider when referring for testing for a genetic dental disorder, and proposes that this subject area should be expanded in the dental undergraduate and postgraduate curricula in the UK.

Entities:  

Mesh:

Year:  2018        PMID: 29795503     DOI: 10.1038/sj.bdj.2018.360

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


  20 in total

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Authors:  Laura L Dudlicek; Elizabeth A Gettig; Kenneth R Etzel; Thomas C Hart
Journal:  J Dent Educ       Date:  2004-08       Impact factor: 2.264

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Authors:  Angus Clarke
Journal:  BMJ       Date:  2007-07-07

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Authors:  P S Fleming; G M Xavier; A T DiBiase; M T Cobourne
Journal:  Br Dent J       Date:  2010-01-09       Impact factor: 1.626

4.  Randomized trial of the anti-FGF23 antibody KRN23 in X-linked hypophosphatemia.

Authors:  Thomas O Carpenter; Erik A Imel; Mary D Ruppe; Thomas J Weber; Mark A Klausner; Margaret M Wooddell; Tetsuyoshi Kawakami; Takahiro Ito; Xiaoping Zhang; Jeffrey Humphrey; Karl L Insogna; Munro Peacock
Journal:  J Clin Invest       Date:  2014-02-24       Impact factor: 14.808

5.  No expectation to share incidental findings in genomic research.

Authors:  Anna Middleton; Katherine I Morley; Eugene Bragin; Helen V Firth; Matthew E Hurles; Caroline F Wright; Michael Parker
Journal:  Lancet       Date:  2014-12-17       Impact factor: 79.321

6.  Association of GLUT2 and TAS1R2 genotypes with risk for dental caries.

Authors:  G V Kulkarni; T Chng; K M Eny; D Nielsen; C Wessman; A El-Sohemy
Journal:  Caries Res       Date:  2012-12-19       Impact factor: 4.056

Review 7.  Future developments in XLHED treatment approaches.

Authors:  Kenneth Huttner
Journal:  Am J Med Genet A       Date:  2014-03-26       Impact factor: 2.802

8.  Asfotase alfa therapy for children with hypophosphatasia.

Authors:  Michael P Whyte; Katherine L Madson; Dawn Phillips; Amy L Reeves; William H McAlister; Amy Yakimoski; Karen E Mack; Kim Hamilton; Kori Kagan; Kenji P Fujita; David D Thompson; Scott Moseley; Tatjana Odrljin; Cheryl Rockman-Greenberg
Journal:  JCI Insight       Date:  2016-06-16

9.  Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland.

Authors:  M Hietala; A Hakonen; A R Aro; P Niemelä; L Peltonen; P Aula
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

10.  The challenges of genome analysis in the health care setting.

Authors:  Anneke Lucassen; Richard S Houlston
Journal:  Genes (Basel)       Date:  2014-07-22       Impact factor: 4.096

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