Literature DB >> 9643255

Oligodontia--a case report.

P F Tsai1, H R Chiou, C C Tseng.   

Abstract

Oligodontia is defined as the congenital absence of six or more teeth, excluding the third molars. Genetic factors play an important role in oligodontia, which can occur as an isolated finding or as part of a syndrome. Characteristic dental symptoms are a reduced number of teeth, a reduction in tooth size, anomalies of tooth form, and delayed eruption. This article describes treatment of a 6-year-old girl with congenital absence of 16 permanent teeth. Her malocclusion was corrected by orthodontic therapy, and removable partial dentures were made to improve esthetics and chewing function.

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Year:  1998        PMID: 9643255

Source DB:  PubMed          Journal:  Quintessence Int        ISSN: 0033-6572            Impact factor:   1.677


  5 in total

1.  Familial ectodermal dysplasia: a peers' agony.

Authors:  Karthik Hegde; Roopashri Rajesh Kashyap; Gopakumar Nair; Preeti P Nair
Journal:  BMJ Case Rep       Date:  2013-07-23

2.  Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies.

Authors:  Derya Ceyhan; Zuhal Kirzioglu; Nilufer Sahin Calapoglu
Journal:  Indian J Dent       Date:  2014-10

3.  An unusual occurrence of multiple dental anomalies in a single nonsyndromic patient: a case report.

Authors:  N B Nagaveni
Journal:  Case Rep Dent       Date:  2012-06-25

4.  Nonsyndromic oligodontia in siblings: A rare case report.

Authors:  Veerabadhran Mahesh Mathian; Murugesan Gawthaman; Ramachandran Karunakaran; Selvaraj Vinodh; Sundaram Manikandan; Alagappan Meenakshi Sundaram
Journal:  J Pharm Bioallied Sci       Date:  2014-07

5.  Permanent Maxillary Canine Agenesis: A Rare Case Report.

Authors:  Halaswamy V Kambalimath; Somya Jain; Raju Umaji Patil; Alexander Asokan; Deepashri Kambalimath
Journal:  Int J Clin Pediatr Dent       Date:  2015-09-11
  5 in total

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