Results 31 to 40 of about 4,466 (206)

Severe hypodontia in a set of triplets [PDF]

open access: yesBritish 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   +3 more
openaire   +3 more sources

COMPLEX ORTHODONTIC-IMPLANT TREATMENT IN INCISOR HYPODONTIA CASES [PDF]

open access: yesJournal of IMAB, 2020
Purpose:The purpose of the current paper is to show clinical cases with unilateral and bilateral incisal hypodontia, treated with complex orthodontic – implant treatment.
Miroslava Dinkova
doaj   +1 more source

The prevalence and distribution of hypodontia in a sample of Qatari patients

open access: yesJournal of Orthodontic Science, 2016
Objective: The aims of this study were to determine the prevalence of hypodontia in the permanent dentition in a sample of Qatari patients attending a dental center and to compare the results with the reported findings of other populations.
Hayder Abdalla Hashim, Sozan Al-Said
doaj   +1 more source

Management of hypodontia [PDF]

open access: yesBritish Dental Journal, 2006
Objective To analyse the clinical performance and factors influencing the survival of resin-bonded bridgework provided for hypodontia patients with missing maxillary lateral incisors, following orthodontic treatment to open, maintain or redistribute the missing tooth space.
openaire   +2 more sources

Effects of hypodontia on craniofacial structures and mandibular growth pattern

open access: yesHead & Face Medicine, 2011
Introduction This study was performed to examine craniofacial structures in persons with hypodontia and to reveal any differences, that may occur, when agenetic teeth are only found in the maxilla, the mandible or in both jaws.
Kreczi Amelia   +3 more
doaj   +1 more source

Prevalence and Pattern of Hypodontia among Croatian Orthodontic Patients

open access: yesActa Stomatologica Croatica, 2020
Objective: The objective of this retrospective study was to assess the prevalence of hypodontia in the permanent dentition among Croatian orthodontic patients. The occurrence was evaluated concern-ing gender, specific missing teeth, the location, pattern
Daša Nikolov Borić   +3 more
doaj   +1 more source

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

open access: yesDental 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   +1 more
doaj   +1 more source

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

open access: yesBrazilian 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   +4 more
doaj   +1 more source

Prevalence of Hypodontia in a Sample of Spanish Dental Patients

open access: yesActa 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   +4 more
doaj   +1 more source

Wilms Tumor in Children with AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala   +9 more
wiley   +1 more source

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