Results 51 to 60 of about 8,907 (247)
Management of hypodontia [PDF]
British Dental Journal, 2006 Objective To analyse the clinical performance and factors influencing the survival of resin-bonded bridgework provided for hypodontia patients with missing maxillary lateral incisors, following orthodontic treatment to open, maintain or redistribute the missing tooth space.
openaire +2 more sources
A rare case of congenital absence of permanent canines associated with other dental anomalies [PDF]
, 2011 Agenesis of permanent canines is a rare condition and that of both maxillary and mandibular permanent canines is extremely rare. Reports of such cases are very scarce in the literature.
Dutta, B. +2 more
core +1 more source
Effects of hypodontia on craniofacial structures and mandibular growth pattern
Head & Face Medicine, 2011 Introduction This study was performed to examine craniofacial structures in persons with hypodontia and to reveal any differences, that may occur, when agenetic teeth are only found in the maxilla, the mandible or in both jaws.
Kreczi Amelia +3 more
doaj +1 more source
Prevalence and Pattern of Hypodontia among Croatian Orthodontic Patients
Acta Stomatologica Croatica, 2020 Objective: The objective of this retrospective study was to assess the prevalence of hypodontia in the permanent dentition among Croatian orthodontic patients. The occurrence was evaluated concern-ing gender, specific missing teeth, the location, pattern
Daša Nikolov Borić +3 more
doaj +1 more source
Association between hypodontia of permanent maxillary lateral incisors and other dental anomalies
Dental Press Journal of Orthodontics, 2021 Introduction: Tooth agenesis is often associated with other tooth anomalies, such as microdontia, delayed eruption and ectopic eruption. Moreover, they may be found all in the same individual, as certain genetic mutations may have a variable phenotypic ...
Diego Junior da Silva Santos +1 more
doaj +1 more source
American Journal of Medical Genetics Part A, EarlyView.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
Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia [PDF]
, 2016 Dental anomalies are not an unusual finding in routine dental examination. The effect of dental anomalies can lead to functional, esthetic and occlusal problems.
Yassin, Syed M.
core +1 more source
Absence of mutations in the promoter region of the lef1 gene in Patients with hypodontia
Brazilian Journal of Oral Sciences, 2015 Hypodontia, the congenital absence of one or a few permanent teeth, is one of the most frequent alterations of the human dentition. Although hypodontia does not represent a public health problem, it may cause both, speech and masticatory dysfunction as ...
Elisângela R. Silva +4 more
doaj +1 more source
Pediatric Blood &Cancer, EarlyView.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
Prevalence of Hypodontia in a Sample of Spanish Dental Patients
Acta Stomatologica Croatica, 2018 Objectives: The aim of this retrospective study was to evaluate the prevalence of hypodontia in a sample of dental patients, aged between seven and eleven years at University Alfonso X in Madrid (Spain).
Rebeca Ayala Sola +4 more
doaj +1 more source