Results 81 to 90 of about 9,160 (248)
Multiple crown size variables of the upper incisors in patients with supernumerary teeth compared with controls [PDF]
, 2009 Aims: As part of ongoing studies of the aetiology of dental anomalies the aims of this study were to identify multiple components of tooth size of the upper permanent incisors in 34 patients with supernumerary teeth and to compare them with those in a ...
Brook, AH +3 more
core +2 more sources
Indian Journal of Dental Sciences, 2019 Aim: This study was aimed to compare Bolton's ratio and the arch width of patients with hypodontia with that of the control group. Materials and Methods: Ten cases with congenitally missing teeth and 10 cases of the control group were grouped in this ...
Deepankar Bhatnagar +4 more
doaj +1 more source
TRENDS IN DENTAL CARE FOR INDIVIDUALS WITH ECTODERMAL DYSPLASIA [PDF]
, 2011 Purpose: The specific aim of this study is to evaluate the trends in dental health care for individuals with ectodermal dysplasia. Methods: This was a cross sectional analysis of subjects recruited through the National Foundation of Ectodermal Dysplasia (
Edwards, Justin
core +1 more source
Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis
Australasian 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
Familial Hypodontia: A Case Series
Kathmandu University Medical Journal, 2017 The phenomenon of congenitally missing teeth has been described with different names: hypodontia, oligodontia, anodontia, congenitally missing teeth and dental agenesis. The present paper reports familial hypodontia, involving two siblings from a single family.
T L Ravishankar +3 more
openaire +3 more sources
Special Care in Dentistry, Volume 45, Issue 3, May/June 2025.ABSTRACT Aim To identify the behavioral correlates of caregiver‐reported oral health of individuals with Joubert Syndrome (JS). Methods This cross‐sectional study included 302 caregivers of individuals with JS from the JS registry who responded to a 56‐item REDCap survey, and a purposive subset of 30 participants with JS for which a dental screening ...
Sai Win Kyaw Htet Aung +6 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
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 +3 more sources
“Mini Molar Tooth” Sign in POLR3B‐Associated Cerebellar Ataxia with Hypomyelinating Leukodystrophy
Movement Disorders Clinical Practice, Volume 12, Issue 10, Page 1659-1661, October 2025.
Luca Marsili +5 more
wiley +1 more source
Clinical Oral Implants Research, Volume 36, Issue 4, Page 505-517, April 2025.ABSTRACT Objectives WNT10A mutations are associated with tooth agenesis. This study aimed to assess the clinical outcomes of dental implants in patients carrying WNT10A mutations with different molecular statuses and phenotypes over a long‐term follow‐up period. Materials and Methods Patients with tooth agenesis were screened by whole‐exome sequencing (
Jiaqi Dou +6 more
wiley +1 more source