Results 1 to 10 of about 12,379 (290)
Association between Sella Turcica Bridging and Hypodontia - A Radiographic Study
Background: The bridging of sella turcica and dental anomalies have common embryonic origins and underlying genetic basis. Many studies have linked sella turcica bridging to developmental syndromes affecting the craniofacial region, and local dental ...
S. Gupta, Shristi Rauniyar
semanticscholar +1 more source
A multidisciplinary approach for the management of hypodontia: case report
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 +6 more
doaj +1 more source
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
Familial cases of missing mandibular incisor: three case presentations [PDF]
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
Assessment of information resources for people with hypodontia [PDF]
Aim: To assess the adequacy of patient information to support understanding and decision-making for people affected by hypodontia. Methods: 1) Questionnaire to understand the provision of patient information by dentists; 2) Systematic search to ...
A Harwood +21 more
core +1 more source
Removable Partial Dentures vs Overdentures in Children with Ectodermal Dysplasia: Two Case Reports [PDF]
Ectodermal dysplasia (ED) represents a disorder group characterised by abnormal development of the ectodermal derivatives. Removable partial dentures (RPD), complete dentures (CD) or overdentures (OD) are most often the treatment of choice for young ...
Angelopoulou, Matina V. +3 more
core +1 more source
Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis. [PDF]
Mutations of the Ectodysplasin-A (EDA) gene are generally associated with the syndrome hypohidrotic ectodermal dysplasia (MIM 305100), but they can also manifest as selective, non-syndromic tooth agenesis (MIM300606).
A Monreal +40 more
core +3 more sources
Severe hypodontia in a set of triplets [PDF]
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 +3 more
openaire +2 more sources
Development and assessment of reliable patient-based hypodontia website
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
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

