Genetic testing for amelogenesis imperfecta: knowledge and attitudes of paediatric dentists

被引:8
作者
McDowall, F. [1 ,2 ]
Kenny, K. [1 ]
Mighell, A. J. [3 ]
Balmer, R. C. [1 ,2 ]
机构
[1] Univ Leeds, Leeds Dent Inst, Paediat Dent Dept, Leeds, W Yorkshire, England
[2] Harrogate & Dist Fdn Trust, North Yorkshire Community Dent Serv, Harrogate, N Yorkshire, England
[3] Univ Leeds, Leeds Sch Dent, Oral Med Dept, Leeds, W Yorkshire, England
关键词
CLASSIFICATION; MUTATIONS;
D O I
10.1038/sj.bdj.2018.641
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction Genetic testing is increasingly applied across healthcare reflecting the value to diagnosis, clinical decision-making, service organisation and advancement of the research-informed evidence base. Patient expectations are changing. Genetic testing has not been part of dental practice. Introduction of an NHS-targeted gene panel test for amelogenesis imperfecta (Al), a heterogeneous genetic disorder affecting enamel appearance and function, represents a paradigm shift. This impacts on specialists in paediatric dentistry and other members of the dental team delivering longitudinal care for individuals with Al. Aim To evaluate the opinions of paediatric dentists on genetic testing for dental conditions using Al as the exemplar. Method Two focus groups of nine UK NHS paediatric dentists each were audio recorded (September 2016) and transcribed verbatim. Qualitative analysis was undertaken using Interpretative Phenomenological Analysis (IPA). Results A wide range of views reflected existing insight and understanding. Three core concepts of justification, ownership and challenges emerged. The clinicians were generally open to involvement with genetic testing in paediatric dentistry, but required more support. Conclusion Areas for clarification and professional development were identified as important in ensuring that genetic testing in dentistry, which is currently in its infancy, reaches translational potential and enhances patient care as this area of healthcare continues to advance rapidly.
引用
收藏
页码:335 / 339
页数:5
相关论文
共 15 条
  • [1] Amelogenesis imperfecta: a classification and catalogue for the 21st century
    Aldred, MJ
    Savarirayan, R
    Crawford, PJM
    [J]. ORAL DISEASES, 2003, 9 (01) : 19 - 23
  • [2] [Anonymous], 2016, GENE DOSSIER 331 AME
  • [3] The psychosocial impact of developmental dental defects in people with hereditary amelogenesis imperfecta
    Coffield, KD
    Phillips, C
    Brady, M
    Roberts, MW
    Strauss, RP
    Wright, JT
    [J]. JOURNAL OF THE AMERICAN DENTAL ASSOCIATION, 2005, 136 (05) : 620 - 630
  • [4] Amelogenesis imperfecta
    Crawford, Peter J. M.
    Aldred, Michael
    Bloch-Zupan, Agnes
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2007, 2 (1)
  • [5] Interventions for the restorative care of amelogenesis imperfecta in children and adolescents
    Dashash, Mayssoon
    Yeung, C. Albert
    Jamous, Issam
    Blinkhorn, Anthony
    [J]. COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2013, (06):
  • [6] Davies SC, 2017, Annual report of the chief medical officer. Generation genome
  • [7] Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations
    de la Dure-Molla, Muriel
    Quentric, Mickael
    Yamaguti, Paulo Marcio
    Acevedo, Ana-Carolina
    Mighell, Alan J.
    Vikkula, Miikka
    Huckert, Mathilde
    Berdal, Ariane
    Bloch-Zupan, Agnes
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2014, 9
  • [8] Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations
    Jaureguiberry, Graciana
    De la Dure-Molla, Muriel
    Parry, David
    Quentric, Mickael
    Himmerkus, Nina
    Koike, Toshiyasu
    Poulter, James
    Klootwijk, Enriko
    Robinette, Steven L.
    Howie, Alexander J.
    Patel, Vaksha
    Figueres, Marie-Lucile
    Stanescu, Horia C.
    Issler, Naomi
    Nicholson, Jeremy K.
    Bockenhauer, Detlef
    Laing, Christopher
    Walsh, Stephen B.
    McCredie, David A.
    Povey, Sue
    Asselin, Audrey
    Picard, Arnaud
    Coulomb, Aurore
    Medlar, Alan J.
    Bailleul-Forestier, Isabelle
    Verloes, Alain
    Le Caignec, Cedric
    Roussey, Gwenaelle
    Guiol, Julien
    Isidor, Bertrand
    Logan, Clare
    Shore, Roger
    Johnson, Colin
    Inglehearn, Christopher
    Al-Bahlani, Suhaila
    Schmittbuhl, Matthieu
    Clauss, Franois
    Huckert, Mathilde
    Laugel, Virginie
    Ginglinger, Emmanuelle
    Pajarola, Sandra
    Sparta, Giuseppina
    Bartholdi, Deborah
    Rauch, Anita
    Addor, Marie-Claude
    Yamaguti, Paulo M.
    Safatle, Heloisa P.
    Acevedo, Ana Carolina
    Martelli-Junior, Hercilio
    dos Santos Netos, Pedro E.
    [J]. NEPHRON PHYSIOLOGY, 2012, 122 (1-2): : 1 - 6
  • [9] Delivery of a Clinical Genomics Service
    Newman, William G.
    Black, Graeme C.
    [J]. GENES, 2014, 5 (04): : 1001 - 1017
  • [10] How do children with amelogenesis imperfecta feel about their teeth?
    Parekh, Susan
    Almehateb, Mohammad
    Cunningham, Sue J.
    [J]. INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY, 2014, 24 (05) : 326 - 335