Results 31 to 40 of about 4,159 (185)

Impact of Hypodontia on Social Well-Being and Quality of Life of Children

BioMedica, 2020
Background and Objective: The congenital absence of one or more deciduous or permanent teeth is called  hypodontia. It is the most common congenital dental anomaly. Hypodontia could be caused by a number of genetic and environmental factors. The aim
Qurrat-ul-Ain Fatima, Unaiza Jawad, Muhammed Mujtaba, Wali Dad   +3 more
doaj   +1 more source

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

Brazilian 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, Regina C. R. Peres, Raquel M. Scarel-Caminaga, Ferdinando De Conto, Sergio R. P. Line   +4 more
doaj   +1 more source

Congenital Intraoral Synechiae: A Scoping Review of Airway, Feeding, and Surgical Management

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To map the existing literature on congenital intraoral synechiae and summarize reported anatomic patterns, clinical presentation, associated anomalies/syndromes, and outcomes to inform standardized diagnostic and therapeutic approaches. Data Sources PubMed, CINAHL, Embase, Web of Science, and Google Scholar were searched from January
Jason Bernier, Mathieu Bergeron
wiley   +1 more source

Prevalence of Hypodontia in a Sample of Spanish Dental Patients

Acta Stomatologica Croatica, 2018
Objectives: The aim of this retrospective study was to evaluate the prevalence of hypodontia in a sample of dental patients, aged between seven and eleven years at University Alfonso X in Madrid (Spain).
Rebeca Ayala Sola, Pablo Ayala Sola, Javier De La Cruz Pérez, Iván Nieto Sánchez, Inés Díaz Renovales   +4 more
doaj   +1 more source

Rare Novel Genetic Variants of the OFD1 Gene Associated With a Familial Form and a Sporadic Case of Long Bone Atypical Fractures

Clinical Genetics, EarlyView.
A novel rare variant of the OFD1 gene was identified in a family with dental hypoplasia, facial hypoplasia, and adult‐onset multiple atypical fractures of long bones. Another variant of the OFD1 gene was found in a woman with bisphosphonate‐associated atypical femur fracture.
Marie‐Ève Boisvert, Halim Maaroufi, Rachel Laframboise, Frédéric Fournier, Suzanne N. Morin, Edith Gagnon, Claudia Gagnon, Fabrice Mac‐Way, Mahmoud Rouabhia, Louis‐Georges Ste‐Marie, Arnaud Droit, Jacques P. Brown, Laëtitia Michou   +12 more
wiley   +1 more source

Association between hypodontia of permanent maxillary lateral incisors and other dental anomalies

Dental Press Journal of Orthodontics, 2021
Introduction: Tooth agenesis is often associated with other tooth anomalies, such as microdontia, delayed eruption and ectopic eruption. Moreover, they may be found all in the same individual, as certain genetic mutations may have a variable phenotypic ...
Diego Junior da Silva Santos, José Augusto Mendes Miguel   +1 more
doaj   +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

Progress 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, Ali Alaqla, Bader Almuzzaini, Mohammed Aldrees, Ghaida Alnaqa, Farah Almasoud, Omar Aldibasi, Hala Alshamlan   +7 more
doaj   +1 more source

A multidisciplinary approach for the management of hypodontia: case report

Journal 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, Fabio C Lorenzoni, Leandro Moura Martins, Caio Vinícius Martins do Valle, José Fernando Castanha Henriques, Ana Lúcia Pompéia Fraga de Almeida, Luiz Fernando Pegoraro   +6 more
doaj   +1 more source

Severe hypodontia in a set of triplets [PDF]

British Dental Journal, 2006
Hypodontia is the developmental absence of one or more teeth from the dentition and constitutes one of the most common developmental anomalies in humans with a reported prevalence of 1.6 to 9.6% in the permanent dentition. Hypodontia may occur in association with other genetic diseases, or as an isolated familial or sporadic form.
S O, Adeboye, B O I, Cole, R S, Hobson, M J, Wright   +3 more
openaire   +2 more sources

Association Between Hypomineralisation of Second Primary Molars and Tooth Agenesis

International Journal of Paediatric Dentistry, EarlyView.
ABSTRACT Background Hypomineralisation of second primary molars (HSPM) is an enamel defect with a multifactorial and potentially genetic aetiology. While the association between enamel defects and dental anomalies is a relatively recent area of investigation, it has not yet been explored specifically in cases of HSPM.
Débora Juliana de Araújo Lopes, Eloisa Cesario Fernandes, Jaderson Felipe Santos Dantas, Patrícia Bittencourt Santos   +3 more
wiley   +1 more source