Results 61 to 70 of about 12,486 (245)

Absence of mutations in the promoter region of the lef1 gene in Patients with hypodontia

open access: yesBrazilian 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

A rare case of congenital absence of permanent canines associated with other dental anomalies [PDF]

open access: yes, 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

Non-syndromic hypodontia (NSH) in permanent teeth – epidemiological study [PDF]

open access: yesRomanian Journal of Stomatology, 2020
Aim. Assessment of characteristics of non-syndromic hypodontia (NSH) in permanent teeth (PT) in a group of Romanian children and adolescents. Material and method. Descriptive retrospective observational study on dental files and orthopantomograms of 138
Ioana-Andreea Stanciu   +5 more
doaj   +1 more source

Rethinking brachycephaly: Anatomical implications and health considerations in lagomorphs

open access: yesThe Anatomical Record, EarlyView.
Abstract Brachycephaly in domestic rabbits is increasingly perceived by welfare organizations as associated with significant health complications, particularly oral pathologies. Despite this perception, comparative anatomical research into rabbit brachycephaly is limited compared to that of dogs and cats, compelling an in‐depth examination of its ...
Helaina Cressy   +3 more
wiley   +1 more source

Association between Sella Turcica Bridging and Hypodontia - A Radiographic Study

open access: yes, 2020
Background: The bridging of sella turcica and dental anomalies have common embryonic origins and underlying genetic basis. Many studies have linked sella turcica bridging to developmental syndromes affecting the craniofacial region, and local dental ...
S. Gupta, Shristi Rauniyar
semanticscholar   +1 more source

A multidisciplinary approach for the management of hypodontia: case report

open access: yesJournal of Applied Oral Science, 2011
Hypodontia is the congenital absence of one or more teeth and may affect permanent teeth. Several options are indicated to treat hypodontia, including the maintenance of primary teeth or space redistribution for restorative treatment with partial ...
Accácio Lins do Valle   +6 more
doaj   +1 more source

Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia [PDF]

open access: yes, 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

Optimizing Hard and Soft‐Tissue Esthetics With Anterior Cantilever Zirconia Ceramic Resin‐Bonded Fixed Dental Prostheses

open access: yesJournal of Esthetic and Restorative Dentistry, EarlyView.
ABSTRACT Objective The replacement of missing maxillary lateral incisors poses both functional and esthetic challenges, not only from a restorative but also from a periodontal aspect. This case report presents a step‐by‐step protocol for ideal hard and soft‐tissue esthetics with cantilever zirconia ceramic resin‐bonded fixed dental prostheses (RBFDPs).
Markus B. Blatz   +3 more
wiley   +1 more source

Delayed Dental Development in Children With Non‐Syndromic Hypodontia: A Cross‐Sectional Study Using a Machine Learning Approach to Dental Age Estimation

open access: yesOrthodontics &Craniofacial Research, EarlyView.
ABSTRACT Objectives To investigate the influence of non‐syndromic hypodontia on radiographic dental development and to estimate dental age in children with bilateral mandibular agenesis using a machine learning approach. Materials and Methods This retrospective cross‐sectional study included 626 children aged 6–15 years (311 with dental agenesis, 315 ...
Marine Crosnier   +3 more
wiley   +1 more source

What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients

open access: yesProgress in Orthodontics
Background Hypodontia is the most prevalent dental anomaly in humans, and is primarily attributed to genetic factors. Although genome-wide association studies (GWAS) have identified single-nucleotide polymorphisms (SNP) associated with hypodontia ...
Nora Alhazmi   +7 more
doaj   +1 more source

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