Results 101 to 110 of about 11,727 (288)
Česká Stomatologie a Praktické Zubní Lékařství, 2012 Background: Tooth agenesis means absence or incomplete development of tooth. It is a common human anomaly, which according to Online Mendelian Inheritance in Man database affects approximately 20% of the population.
L. Gábrlíková
doaj +1 more source
Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review [PDF]
, 2014 Objectives: In the present study, it is described the phenotypical analysis and the mutational screening, for genes PAX9 and MSX1, of six families affected by severe forms of tooth agenesis associated with other dental anomalies and systemic entities ...
Arte, Sirpa +5 more
core +1 more source
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
Craniofacial profile in Southern Chinese with hypodontia [PDF]
The European Journal of Orthodontics, 2009 The association between craniofacial morphology and congenitally missing teeth is at present unclear. The aims of this study were to investigate whether hypodontia is associated with changes in the sagittal skeletal profile and to identify putative relationships between the skeletal profile and the severity of hypodontia.
Chan, DWS, McMillan, AS, Samman, N
openaire +5 more sources
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
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
Non-syndromic occurrence of true generalized microdontia with hypodontia
Medicine, 2019 Rational: Dental abnormalities can occur at any stage of tooth development. Of these abnormalities, true generalized microdontia is a rare condition in which all teeth are smaller than normal, while hypodontia is defined as the absence of 1 to 5 teeth ...
Yuan Chen +4 more
semanticscholar +1 more source
Morphological and numerical characteristics of the southern Chinese dentitions. Part I: anomalies in the permanent dentition [PDF]
, 2010 Aim: To investigate the prevalence of eight morphological and numerical anomalies in the southern Chinese permanent dentition and to compare these with studies from different populations. Materials and Methods: The material used in the study consisted
King, NM, Tsai, JSJ, Wong, HM
core +1 more source
Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature
Pediatric Dermatology, Volume 42, Issue 2, Page 305-310, March/April 2025.ABSTRACT We describe a 1‐day old female with features of keratitis‐ichthyosis‐deafness (KID) syndrome and natal teeth. Genetic analysis confirmed GJB2 263C and A88V de novo pathogenic variants consistent with KID syndrome. Natal teeth were promptly extracted to avoid the risk of aspiration.
Sarah Maarouf +3 more
wiley +1 more source
Seven Novel Variants of Weiss‐Kruszka Syndrome and Phenotype Expansion
American Journal of Medical Genetics Part A, Volume 197, Issue 2, February 2025.ABSTRACT Weiss‐Kruszka syndrome (WKS) is a rare genetic disorder characterized by metopic ridging, ptosis, arched eyebrows, down slanting palpebral fissures, abnormalities in the corpus callosum, cardiac malformations, and variable neurodevelopmental delay. To date, 32 individuals with a diagnosis of WKS have been reported in the literature.
Anna Hau +7 more
wiley +1 more source