Literature DB >> 6362744

Classification and genetics of numeric anomalies of dentition.

N J Burzynski, V H Escobar.   

Abstract

A suggested classification of numeric anomalies of teeth is a trimodal classification: anodontia, hypodontia, and hyperdontia. A subclassification into nonsyndromic and syndromic cases would allow for uniform analysis. The limited data on anodontia and hyperdontia have made the genetic analysis of these anomalies difficult. The most suitable data for analysis on the genetics of numeric anomalies of dentition are on hypodontia. A reevaluation of this data, as presented in this report, suggests hypodontia follows an autosomal dominant mode of inheritance. However, the fact that penetrance is not complete suggests the presence of a mechanism whereby epistatic genes interfere with the phenotypic expression of the hypodontia gene. How this occurs is uncertain, but the available evidence suggests a major single gene defect, which is modified by genetic or environmental factors.

Entities:  

Mesh:

Year:  1983        PMID: 6362744

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  20 in total

Review 1.  Developmental disorders of the dentition: an update.

Authors:  Ophir D Klein; Snehlata Oberoi; Ann Huysseune; Maria Hovorakova; Miroslav Peterka; Renata Peterkova
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

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.  A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?

Authors:  Adrianna Mostowska; Barbara Biedziak; Wiesław H Trzeciak
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

4.  A multidisciplinary approach for the management of hypodontia: case report.

Authors:  Accácio Lins do Valle; Fabio C Lorenzoni; Leandro Moura Martins; Caio Vinícius Martins do Valle; José Fernando Castanha Henriques; Ana Lúcia Pompéia Fraga de Almeida; Luiz Fernando Pegoraro
Journal:  J Appl Oral Sci       Date:  2011-10       Impact factor: 2.698

5.  MSX1 gene variant - its presence in tooth absence - a case control genetic study.

Authors:  Naveen Admala Reddy; Gopinath Adusumilli; Raghu Devanna; Saravanan Pichai; Mayur Gobindram Rohra; Sharmila Arjunan
Journal:  J Int Oral Health       Date:  2013-10-26

6.  Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.

Authors:  P Nieminen; S Arte; S Pirinen; L Peltonen; I Thesleff
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

7.  EDA gene mutations underlie non-syndromic oligodontia.

Authors:  S Song; D Han; H Qu; Y Gong; H Wu; X Zhang; N Zhong; H Feng
Journal:  J Dent Res       Date:  2009-02       Impact factor: 6.116

8.  WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

Authors:  Axel Bohring; Thomas Stamm; Christiane Spaich; Claudia Haase; Kerstin Spree; Ute Hehr; Mandy Hoffmann; Susanne Ledig; Saadettin Sel; Peter Wieacker; Albrecht Röpke
Journal:  Am J Hum Genet       Date:  2009-06-25       Impact factor: 11.025

9.  Hypodontia prevalence and pattern in women with epithelial ovarian cancer.

Authors:  Anita Fekonja; Andrej Čretnik; Iztok Takač
Journal:  Angle Orthod       Date:  2014-04-01       Impact factor: 2.079

10.  Prevalence rate of supernumerary teeth among non-syndromic South Indian population: An analysis.

Authors:  M Nazargi Mahabob; G J Anbuselvan; B Senthil Kumar; S Raja; Sucitha Kothari
Journal:  J Pharm Bioallied Sci       Date:  2012-08
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