Results 81 to 90 of about 8,363 (211)
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
The Application of Clinical Genetics, 2018 Ahmed Abu-Siniyeh,1 Omar F Khabour,1 Arwa I Owais2 1Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, Jordan University of Science and Technology, Irbid, Jordan; 2Department of Applied Dental Sciences, Faculty of Applied ...
Abu-Siniyeh A, Khabour OF, Owais AI
doaj
Journal of Nobel Medical College, 2017 Background: Hypodontia is the developmental absence of one or more teeth from the dentition whereas acquired missing teeth are those lost due to carries, periodontal problem or dental trauma.
Shanti Chhetri +2 more
doaj +1 more source
The Prevalence of Oral and Dental Anomalies in Children with Developmental Disturbances [PDF]
, 2002 Raširenost oro-dentalnih anomalija analizirana je u djece sa smetnjama u razvoju. Ispitivanje je provedeno na uzorku od 606 djece u dobi od 5 do 20 godina koji se sastoji od 303 djeteta sa smetnjama u razvoju (SR) i 303 zdrave djece (K). Skupinu djece sa
Domagoj Glavina +3 more
core +1 more source
Hypodontia in orthodontically treated children [PDF]
European Journal of Orthodontics, 2005 The frequency of hypodontia in orthodontically treated children, both male and female, and the association between tooth type, the upper or lower arch, the affected side and Angle's classification were studied using interviews, oral, study cast and panoramic radiographic examinations of 212 patients with a mean age of 12 years 7 months.
openaire +2 more sources
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
Progress in Orthodontics, 2018 Background Tooth agenesis can involve one or more congenitally missing teeth (CMT) and is the most common congenital dental anomalies in humans. Tooth agenesis and reduction of mesiodistal tooth width are reportedly associated, suggesting that the ...
Norihisa Higashihori +4 more
doaj +1 more source
European Oral Research, 2020 Purpose To evaluate the association between third molar (M3) agenesis and hypodontia and oligodontia in pediatric patients by using panoramic radiography.Materials and Methods Panoramic radiographs of 1,471 patients (899 females; 572 males) and 5,884 ...
Meltem Tekbaş Atay +2 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
Hypodontia in the permanent dentition: a study of its prevalence in Malaysian children
Australasian Orthodontic Journal, 1989 An investigation of the prevalence and distribution of hypodontia was carried out in Malaysian children between the ages of five to fifteen years. Hypodontia occurred in 2.8 per cent of these children.
Nik-Hussein Nik Moriah
doaj +1 more source