Results 81 to 90 of about 12,486 (245)
Patient, 2018 ObjectiveOur objective was to develop and test a discrete-choice experiment (DCE) survey to elicit adolescent and parent preferences for dental care for hypodontia (a developmental condition where one or more teeth fail to develop).MethodsThis was a ...
S. Barber +5 more
semanticscholar +1 more source
The Roles of EDA2R in Ageing and Disease
Aging Cell, Volume 24, Issue 12, December 2025.Elevated expression of the ectodysplasin A2 receptor (EDA2R) has been linked to ageing and disease. We appraise the roles of EDA2R in these processes, exploring mechanisms of action, biomarker potential and therapeutic relevance of EDA2R in multiple contexts. ABSTRACT Ageing is a complex biological process driven, in part, by inflammaging.
Gemma Farrington +9 more
wiley +1 more source
Genetic basis of dental agenesis - molecular genetics patterning clinical dentistry [PDF]
, 2013 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 ...
Chhabra, Anuj +2 more
core +1 more source
BioMed Research International, 2019 The etiology of hypodontia is complex, in which both genetic and environmental factors can be related. The main objective of our study was to contribute to elucidating the genetic background of nonsyndromic hypodontia (NSH). In this order, we selected 97
Krisztina Mártha +3 more
semanticscholar +1 more source
Non-syndromic occurrence of true generalized microdontia with hypodontia
Medicine, 2019 Rational: Dental abnormalities can occur at any stage of tooth development. Of these abnormalities, true generalized microdontia is a rare condition in which all teeth are smaller than normal, while hypodontia is defined as the absence of 1 to 5 teeth ...
Yuan Chen +4 more
semanticscholar +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero +17 more
wiley +1 more source
Indian Journal of Dental Sciences, 2019 Aim: This study was aimed to compare Bolton's ratio and the arch width of patients with hypodontia with that of the control group. Materials and Methods: Ten cases with congenitally missing teeth and 10 cases of the control group were grouped in this ...
Deepankar Bhatnagar +4 more
doaj +1 more source
Pediatric Blood &Cancer, Volume 72, Issue 11, November 2025.ABSTRACT Introduction As survival of paediatric cancer improves, more emphasis is placed on late adverse effects. However, the dental and periodontal adverse effects of cancer treatments in children remain an underinvestigated complication. This study aims to investigate the prevalence of late clinical dental adverse effects (cDAE) in survivors of ...
Koen B. Krommenhoek +10 more
wiley +1 more source
Developmental absence of maxillary lateral incisors in the Portuguese population [PDF]
, 2005 The aim of this study was to evaluate the prevalence and clinical manifestation of developmental absence of maxillary permanent lateral incisors in the Portuguese population.
Maciel, P. +3 more
core +2 more sources
TRENDS IN DENTAL CARE FOR INDIVIDUALS WITH ECTODERMAL DYSPLASIA [PDF]
, 2011 Purpose: The specific aim of this study is to evaluate the trends in dental health care for individuals with ectodermal dysplasia. Methods: This was a cross sectional analysis of subjects recruited through the National Foundation of Ectodermal Dysplasia (
Edwards, Justin
core +1 more source