[HTML][HTML] Congenitally missing teeth (hypodontia): A review of the literature concerning the etiology, prevalence, risk factors, patterns and treatment

V Rakhshan - Dental research journal, 2015 - journals.lww.com
Congenitally missing teeth (CMT), or as usually called hypodontia, is a highly prevalent and
costly dental anomaly. Besides an unfavorable appearance, patients with missing teeth may …

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

V Rakhshan - Progress in orthodontics, 2013 - Springer
No meta-analyses or systematic reviews have been conducted to evaluate numerous
potential biasing factors contributing to the controversial results on congenitally missing …

An orthopantomographic study of hypodontia in permanent teeth of Japanese pediatric patients

HA Goya, S Tanaka, T Maeda, Y Akimoto - Journal of oral science, 2008 - jstage.jst.go.jp
Hypodontia of permanent teeth was evaluated from orthopantomograms of 2072 apparently
healthy pediatric patients at The Hospital of Nihon University School of Dentistry at Matsudo …

[HTML][HTML] Prevalence and pattern of hypodontia in the permanent dentition of 3374 Iranian orthodontic patients

F Amini, V Rakhshan, P Babaei - Dental research journal, 2012 - ncbi.nlm.nih.gov
Background: Hypodontia is the most common dental anomaly and might cause clinical
complications. The aim of this study was to assess the prevalence and pattern of congenital …

EDA Gene Mutations Underlie Non-syndromic Oligodontia

S Song, D Han, H Qu, Y Gong, H Wu… - Journal of dental …, 2009 - journals.sagepub.com
Recent studies have detected mutations in the EDA gene, previously identified as causing X-
linked hypohidrotic ectodermal dysplasia (XLHED), in two families with X-linked non …

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis

D Han, Y Gong, H Wu, X Zhang, M Yan, X Wang… - European journal of …, 2008 - Elsevier
Familial non-syndromic hypodontia shows a wide phenotypic heterogeneity and inherits in
an autosomal-dominant, autosomal-recessive or X-linked mode. Mutations in genes PAX9 …

Dental anomaly patterns associated with tooth agenesis

SJ Choi, JW Lee, JH Song - Acta Odontologica Scandinavica, 2017 - Taylor & Francis
Objective: The objective of this study is to evaluate the relationship between tooth agenesis
and the occurrence of other dental anomalies in children and adolescents. Material and …

[HTML][HTML] A review on non-syndromic tooth agenesis associated with PAX9 mutations

NH Fauzi, YD Ardini, Z Zainuddin, W Lestari - Japanese Dental Science …, 2018 - Elsevier
Tooth agenesis in the reduction of tooth number which includes hypodontia, oligodontia and
anodontia is caused by disturbances and gene mutations that occur during odontogenesis …

[PDF][PDF] Tooth agenesis; aetiological factors

A Azzaldeen, N Watted, A Mai, P Borbély… - Journal of Dental and …, 2017 - researchgate.net
Tooth agenesis is the most prevalent craniofacial congenital anomaly in humans. The term
refers to an isolated disorder in the absence of non-dental phenotypes but is also used to …

Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia

R Kist, M Watson, X Wang, P Cairns… - Human Molecular …, 2005 - academic.oup.com
Missing teeth (hypodontia and oligodontia) are a common developmental abnormality in
humans and heterozygous mutations of PAX9 have recently been shown to underlie a …