Results 91 to 100 of about 11,727 (288)

Identification of copy neutral loss of heterozygosity on chromosomes 1p, 1q, and 6p among nonsyndromic cleft lip and/or without cleft palate with hypodontia

open access: yesBMC Oral Health, 2023
Background Nonsyndromic cleft lip and/or without cleft palate (NSCL/P) with or without hypodontia is a common developmental aberration in humans and animals.
Norliana Ghazali   +4 more
doaj   +1 more source

Ancestry and dental development: A geographic and genetic perspective [PDF]

open access: yes, 2017
Objective: In this study, we investigated the influence of ancestry on dental development in the Generation R Study. Methods: Information on geographic ancestry was available in 3,600 children (1,810 boys and 1,790 girls, mean age 9.81±0.35 years) and ...
Dhamo, B. (Brunilda)   +8 more
core   +1 more source

Oral Health Status of Children With a History of Liver Transplantation

open access: yesPediatric Transplantation, Volume 29, Issue 5, August 2025.
This study examines the oral health of children who have undergone liver transplantation, highlighting dental development delays despite similar caries rates compared to their healthy peers. Findings emphasize the need for integrated dental‐medical care, focusing on dental age assessment and early intervention to optimize oral health outcomes in this ...
Güler Burcu Senirkentli   +2 more
wiley   +1 more source

Development of a Discrete-Choice Experiment (DCE) to Elicit Adolescent and Parent Preferences for Hypodontia Treatment

open access: yesPatient, 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

Familial cases of missing mandibular incisor: three case presentations [PDF]

open access: yes, 1999
Hypodontia is the congenital absence of one or more teeth because of agenesis. The most commonly missing teeth are the third molars, the maxillary lateral incisors and the second premolars.
Ngeow, Dr. W.C.
core  

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

Development and assessment of reliable patient-based hypodontia website

open access: yesPatient Preference and Adherence, 2018
Rozana Valiji Bharmal, Ama Johal Oral Bioengineering (Orthodontics), Institute of Dentistry, Bart’s and The London School of Medicine & Dentistry, Queen Mary College, London, UK Background: The aim of the study was to develop a high-quality ...
Bharmal RV, Johal A
doaj  

Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis

open access: yesAustralasian Journal of Dermatology, Volume 66, Issue 3, Page e109-e119, May 2025.
ABSTRACT Paediatric hypotrichosis is the clinical feature of paucity of hair arising congenitally or in early life with the presentation being that of the child whose hair is growing insufficiently. It is a hallmark finding of a diverse group of genodermatoses and sporadic disorders, presenting as either an isolated symptom or in association with ...
Neda So, Leona Yip, David Orchard
wiley   +1 more source

The association between hypodontia and dental development [PDF]

open access: yesClinical Oral Investigations, 2015
In this cross-sectional study, we aimed to investigate the pattern of hypodontia in the Dutch population and determine the association between hypodontia and dental development in children with and without hypodontia, applying three different standards, Dutch, French Canadian, and Belgian, to estimate dental age.We used dental panoramic radiographs ...
Mette A. R. Kuijpers   +7 more
openaire   +3 more sources

Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia

open access: yesBioMed 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

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