Results 61 to 70 of about 6,227 (189)

Dentoalveolar Changes in the Premolar Region After Two Maxillary Expansion Protocols

open access: yesOrthodontics &Craniofacial Research, EarlyView.
ABSTRACT Objectives To evaluate the dentoalveolar effects on the upper first premolars after two maxillary expansion protocols—rapid maxillary expansion (RME) and alternate rapid maxillary expansion and constriction (Alt‐RAMEC)—before and 6 months after treatment.
Jaqueline Peter   +6 more
wiley   +1 more source

The Incidence of Tooth Agenesis in Pediatric Patients in the Olomouc Region

open access: yes, 2014
Aim of the study: Many developmental anomalies can occur in craniofacial region. Dental developmental anomalies, namely hypodontia, are the most often of them.
E. Kaplová   +3 more
core   +1 more source

Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction. [PDF]

open access: yesJ Dent Sci
Tooth development, or odontogenesis, is a complex process in which several molecular pathways play a key role. Recently, microRNAs, a class of approximately 20-nucleotide small RNA molecules that regulate gene expression, have been implicated in the odontogenesis process.
Giovannetti A   +12 more
europepmc   +5 more sources

Evaluation of Eruption Pattern of Second Permanent Molars Following Extraction of Compromised First Permanent Molars in Children and Its Predicting Factors: A Retrospective Radiographic Study

open access: yesOrthodontics &Craniofacial Research, EarlyView.
ABSTRACT Objectives To evaluate eruption pattern, in terms of space closure and alignment of second permanent molars (SPM), following extractions of first permanent molars (FPM) and assess the effect of predicting factors including age at extraction, developmental stage of SPM, angulation of adjacent teeth and presence of third permanent molars (TPM ...
Fanouria Papaioannou   +4 more
wiley   +1 more source

The WNT10A Gene in Ectodermal Dysplasias and Selective Tooth Agenesis [PDF]

open access: yes, 2014
Mutations in the WNT10A gene were first detected in the rare syndrome odonto-onycho-dermal dysplasia (OODD, OMIM257980) but have now also been found to cause about 35-50% of selective tooth agenesis (STHAG4, OMIM150400), a common disorder that mostly ...
Vieira, Alexandre R   +8 more
core   +1 more source

Oral Manifestations of Non Vascular Ehlers‐Danlos Syndrome Cross‐Sectional Study

open access: yesOral Diseases, EarlyView.
ABSTRACT Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of this study was to describe the oral phenotype of patients with non‐vascular Ehlers‐Danlos syndromes compared to healthy controls.
Aude Grand   +4 more
wiley   +1 more source

Periodontal and orthodontic management of impacted canines

open access: yesPeriodontology 2000, EarlyView.
Abstract The maxillary and mandibular canines are described by many clinicians as the “cornerstone” of the arch. When in their optimal position, they play a critical role in providing a well‐balanced occlusal scheme that contributes toward functional as well as neuromuscular stability, harmony, esthetics, and dentofacial balance.
Mohammad Qali   +3 more
wiley   +1 more source

Measurement of tooth size and shape in subjects with hypodontia and a control group using a new image analysis technique. [PDF]

open access: yes, 2000
The literature referred to here provided information concerning the epidemiology of hypodontia and its association with other developmental anomalies.
Al-Sharood, Mohammad H
core  

Molecular and Genetic Basis of Non-Syndromic Tooth Agenesis

open access: yes, 2015
Background: Tooth agenesis represents the most common anomaly of dental development, which according to Online Mendelian Inheritance in Man (OMIM) database, affects approximately 20% of the population.
A. Ševecová   +3 more
core   +1 more source

Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis

open access: yes, 2018
Tooth agenesis is a common craniofacial abnormality in humans and represents failure to develop 1 or more permanent teeth. Tooth agenesis is complex, and variations in about a dozen genes have been reported as contributing to the etiology.
Erdem, A. P.   +17 more
core   +2 more sources

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