Results 21 to 30 of about 2,773 (156)

BMPR2 Variants Underlie Nonsyndromic Oligodontia

, 2023
Oligodontia manifests as a congenital reduction in the number of permanent teeth. Despite the major efforts that have been made, the genetic etiology of oligodontia remains largely unknown. Bone morphogenetic protein receptor type 2 (BMPR2) variants have
Hailan Feng, Miao Yu, Yu, Miao, Liu, Hangbo, Lin, Bichen, Hangbo Liu, Zheng, Jinglei, Dong Han, Liu, Yang, Yang Liu, Liu, Haochen, Kai Sun, Feng, Hailan, Bichen Lin, Sun, Kai, Haochen Liu, Jinglei Zheng, Han, Dong   +17 more
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Disturbances of dental development distinguish patients with oligodontia-ectodermal dysplasia from isolated oligodontia [PDF]

, 2017
Structured Abstract: Objective: To investigate phenotypic differences in dental development between isolated oligodontia and oligodontia-ectodermal dysplasia (ED). Setting and sample population: A total of 129 patients diagnosed with isolated oligodontia
C. Boxum, E. M. Ongkosuwito, Wolvius, E.B. (Eppo), M. A. R. Kuijpers, Ongkosuwito, E.M. (Edwin), I. Balk-Leurs, Kuijpers, M.A.R. (Mette), Boxum, C. (C.), Dhamo, B. (Brunilda), E. B. Wolvius, B. Dhamo, Balk-Leurs, I. (I.)   +11 more
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Interdisciplinary dental management of patient with oligodontia and maxillary hypoplasia: a case report

BMC Oral Health, 2022
Background The craniofacial developmental abnormality can significantly complicate the oral rehabilitation of patients with oligodontia. This case report describes an interdisciplinary approach that took 7 years to successfully treat a young patient with
Sharon Aronovich, Yuan-Lynn Hsieh, Richard Scott Conley, Bradley Stieper, Marilia Yatabe, Fei Liu   +5 more
doaj   +1 more source

New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742‐2A>G

Molecular Genetics & Genomic Medicine, 2023
Background Ectodermal dysplasias are inherited disorders, which are characterized by congenital defects in two or more ectodermal structures such as skin, sweat glands, hair, nails, teeth, and mucous membranes.
Vivian Reinhold, Stina Syrjänen, Minna Kankuri‐Tammilehto   +2 more
doaj   +1 more source

Dental arch dimensions in oligodontia patients

INTRODUCTION: The aim of this study was to compare the dental arch sizes in a group of oligodontia patients with a group of age- and sex-matched untreated Class I control patients.
Bu X, Hobson RS, Khalaf K
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Estimation of dental age in children in a Turkish population with tooth agenesis

Contemporary Pediatric Dentistry, 2023
Aim: The aim of this study was to investigate tooth development according to chronological age in children with tooth agenesis and to determine whether the severity of tooth agenesis (hypodontia and oligodontia) has an effect on tooth development ...
Canan Bayraktar Nahir, Zuhal Kirzioglu
doaj   +1 more source

Rehabilitation Considerations for Very Young Children with Severe Oligodontia due to Ectodermal Dysplasia: Report of Three Clinical Cases with a 2-Year Follow-Up

Case Reports in Dentistry, 2022
Introduction. Management of oligodontia can be complicated and requires multidiscipline care, involving a wide spectrum of interventions. The aim of this report is to describe the challenges of oral rehabilitation of three very young children with ...
Kyriaki Seremidi, Antigoni Markouli, Andreas Agouropoulos, Nick Polychronakis, Sotiria Gizani   +4 more
doaj   +1 more source

Dental Management of Hypohydrotic Ectodermal Dysplasia: A Case Report [PDF]

Journal of Mashhad Dental School, 2020
Introduction: Ectodermal dysplasia is a genetic rare disease, consisting of a group of abnormalities which are the results of the abnormal development of two or more embryonic ectoderm derivatives, such as the skin, hair, nail, sweat gland, tooth, and ...
Koorosh teymoornezhad, khashayar sanjari, Hosna ebrahimi zadeh   +2 more
doaj   +1 more source

Analysis of AXIN2 gene mutations in a family with isolated oligodontia

口腔疾病防治, 2016
Objective To investigate the mutational characteristics of AXIN2 gene in a family affected by non⁃syn⁃ dromic oligodontia and to provide a molecular basis for studying the pathogenesis of oligodontia.
QIN Han, XU Hong⁃zhi, GONG Yong⁃ qing   +2 more
doaj   +1 more source

EDA Gene Mutations Underlie Non-syndromic Oligodontia [PDF]

, 2009
Recent studies have detected mutations in the EDA gene, previously identified as causing X-linked hypohidrotic ectodermal dysplasia (XLHED), in two families with X-linked non-syndromic hypodontia.
Wu, H., Qu, H., Gong, Y., Han, D., Zhang, X., Song, S., Feng, H., Zhong, N.   +7 more
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