Genetic basis of dental agenesis--molecular genetics patterning clinical dentistry.

Abstract:

:Tooth agenesis is one of the most common congenital malformations in humans. Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be associated with a syndrome (syndromic hypodontia), highlighting the heterogeneity of the condition. Though much progress has been made to identify the developmental basis of tooth formation, knowledge of the etiological basis of inherited tooth loss is still lacking. To date, the mutation spectra of non-syndromic form of familial and sporadic tooth agenesis in humans have revealed defects in various such genes that encode transcription factors, MSX1 and PAX9 or genes that code for a protein involved in canonical Wnt signaling (AXIN2), and a transmembrane receptor of fibroblast growth factors (FGFR1). The aim of this paper is to review the current literature on the molecular mechanisms responsible for selective hypodontia in humans and to present a detailed overview of causative genes and syndromes associated with hypodontia.

authors

Chhabra N,Goswami M,Chhabra A

doi

10.4317/medoral.19158

subject

Has Abstract

pub_date

2014-03-01 00:00:00

pages

e112-9

issue

2

eissn

1698-4447

issn

1698-6946

pii

19158

journal_volume

19

pub_type

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