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Modern Dentistry - Genetic Perspective
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MODERN DENTISTRY- A GENETIC PRESPECTIVE
Mathew George
Dept. of Orthodontics, Mar Baselios Dental College, Cochin

Corresponding Address :


Dr.Mathew George, Senior lecturer -Dept. of Orthodontics, Mar Baselios Dental College, Thankalam, Kothamangalam, Pin Code-686 691, Cochin -Kerala.
E-mail - mathew.orthodon@gmail.com

Introduction

The relative importance of environment and heredity in the development of various diseases and conditions is still a debatable topic. Most of the dental problems are found to have an interaction of these two factors. Many of the genetic disorders involve orofacial region and it is therefore of utmost importance for the dental surgeons to understand the normal development and mechanism involved in the development of abnormalities. We can consider hereditary head and neck pathology in a traditional sense as being either simple or complex consideration.

  • Simple considerations are those resulting from single gene defect.
  • Complex considerations are those which result from a collection of altered genes interacting with environmental influences.

Simple hereditary conditions:
Normal development and maintenance of the craniofacial complex is highly regulated at the molecular level. Odontogenesis can thus have simple gene disorders.

Congenitally missing teeth:
Hypodontia is the most common simple hereditary trait affecting oral cavity with maxillary lateral and premolar being most commonly involved excluding 3rd molars. Several genetic mutations resulting in hypodontia have been identified. The missense mutation in MSX1 gene causes an autosomal dominant trait of variably missing lateral incisors, second premolars and 3rd molars. Mutation in PAX 9 gene has been associated with unusual pattern of hypodontia converting of missing mandibular incisors, molars premolars.

Disorder Inheritance Gene Chromosomal map location
Hypodontia Autosomal dominant MS x 1 4p16
Hypodontia Autosomal dominant PA X 9 14q12 -q13
Anhidrotic ectodermal dysplasia X linked EDA 1 Xq12-q13
Anhidrotic ectodermal dysplasia Autosomal recessive EDA 2 2q11-q13
Anhidrotic ectodermal dysplasia Autosomal dominant EDA 3 2q11-q13

Condition Characteristics Gene Chromosomal map location
Amelogenesis
imperfecta 1
(AIH-1)
Thin enamel with rough surface AMELX Xp22mp
Amelogenesis
imperfecta 2
Yellowish white teeth or opaque teeth AMBN 4q11-q21
Amelogenesis
Imperfecta 3
(AIH 3)
Hypoplastic enamel   Xq22-q28
Osteogenesis
imperfecta
type III and IV associated dentinogenesis imperfecta COLIA 1 & 2 17q21-q22
7q22
Dentinogenesis
imperfecta
Opalescent dentin   4q31-q21
Cleidocranial
dysplasia
Brachycephaly, delayed closure of fontanelles, wormian bone   6p21
Gardner's
syndrome
Osteomas of frontal bone, maxilla, mandible odontomas, unerupted supernumerary teeth APC 5q21


 
 
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