Literature DB >> 8057193

Symptomatology of patients with oligodontia.

Y Schalk-van der Weide1, F A Beemer, J A Faber, F Bosman.   

Abstract

The aims of the present study were: (i) to identify the association of patterns of congenitally missing teeth with combinations of ectodermal symptoms occurring in patients with oligodontia; and (ii) to propose a diagnostic scheme for the general practitioner. For this study 167 patients with oligodontia, both isolated and as part of a syndrome, and 135 healthy controls were interviewed and documented. Chi-square tests, logistic regression and correspondence analysis were used to evaluate and test differences between the groups and associations between the congenitally missing teeth and ectodermal symptoms. No significant differences were found between the control group and the patients with isolated oligodontia with exception of the skin. It could be concluded from the present study that there were no clear associations between congenitally missing teeth, either individually or patterns, and the ectodermal symptoms or combinations of ectodermal symptoms. However, it could be concluded that if the most stable teeth are missing, or if the number of missing teeth is large the patient should be examined carefully for symptoms of ectodermal dysplasia. Using logistic regression a patient could be classified as having isolated oligodontia or oligodontia as part of a syndrome with a specificity and sensitivity of 88.2%.

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Mesh:

Year:  1994        PMID: 8057193     DOI: 10.1111/j.1365-2842.1994.tb01141.x

Source DB:  PubMed          Journal:  J Oral Rehabil        ISSN: 0305-182X            Impact factor:   3.837


  14 in total

1.  Non-syndromic oligodontia of primary and permanent dentition: 5 year follow up- a rare case report.

Authors:  Joyson Moses; Deepa Gurunathan; B N Rangeeth; K S Kannan
Journal:  J Clin Diagn Res       Date:  2013-02-20

2.  On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members.

Authors:  S P Lyngstadaas; H Nordbo; T Gedde-Dahl; P S Thrane
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

3.  Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.

Authors:  Munefumi Kamamoto; Junichiro Machida; Seishi Yamaguchi; Masashi Kimura; Takao Ono; Peter A Jezewski; Yujiro Higashi; Atsuo Nakayama; Kazuo Shimozato; Yoshihito Tokita
Journal:  Eur J Hum Genet       Date:  2011-03-30       Impact factor: 4.246

Review 4.  Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.

Authors:  Sabine Ruf; Dana Klimas; Mario Hönemann; Sarah Jabir
Journal:  J Orofac Orthop       Date:  2013-07-05       Impact factor: 1.938

5.  Multidisciplinary treatment of non-syndromic oligodontia.

Authors:  Canan Bural; Evren Oztas; Sukru Ozturk; Gulsen Bayraktar
Journal:  Eur J Dent       Date:  2012-04

6.  Oral rehabilitation of a young patient with hypohidrotic ectodermal dysplasia: A clinical report.

Authors:  A Anuroopa; Jafar Abdulla; M Lovely
Journal:  Contemp Clin Dent       Date:  2012-04

7.  Nonsyndromic familial oligodontia with multiple dens invaginatus: a case report of an unusual case.

Authors:  D P Vinuth; Poonam Agarwal; Gunjan Dube; S Abhilash; Pallavi Dube
Journal:  Case Rep Dent       Date:  2013-11-05

Review 8.  Congenitally missing teeth (hypodontia): A review of the literature concerning the etiology, prevalence, risk factors, patterns and treatment.

Authors:  Vahid Rakhshan
Journal:  Dent Res J (Isfahan)       Date:  2015 Jan-Feb

9.  Agenesis of multiple primary teeth and.

Authors:  Svsg Nirmala; Niraj Gokhale; N Sivakumar; Md Akhil Quadar
Journal:  Int J Clin Pediatr Dent       Date:  2013-04-26

Review 10.  Meta-analysis and systematic review of factors biasing the observed prevalence of congenitally missing teeth in permanent dentition excluding third molars.

Authors:  Vahid Rakhshan
Journal:  Prog Orthod       Date:  2013-10-01       Impact factor: 2.750

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