Results 221 to 230 of about 6,152 (269)

Psychosocial and behavioural impact of three clinical presentations of oligodontia in a tertiary hospital.

International Journal of Prosthodontics, 2023
PURPOSE To investigate the psychosocial and behavioural impact of oligodontia across three presentation types and determine if presentation type can infer impact. MATERIALS/METHODS Thirty patients, diagnosed and treated for oligodontia between 2006 and
Wendy Nicholls, Steven Singer
semanticscholar   +1 more source

A multidisciplinary approach for full-mouth rehabilitation in oligodontia : A Clinical Report.

Journal of Oral Implantology, 2023
The absence of teeth in children due to congenital agenesis, syndromic or not, can lead to oral dysfunctions with general repercussions and socio-psychological problems.
Estelle Demes, N. Graillon, F. Afota, C. Savoldelli, R. Lan   +4 more
semanticscholar   +1 more source

Reduced bone dimension in patients affected by oligodontia: A retrospective study on maxillary and mandibular CBCT.

Journal of Clinical Periodontology, 2023
AIM Oligodontia (OD) is a rare developmental condition characterized by the absence of six or more teeth. Dental implant placement may be challenging due to anatomical factors.
Nicolas Dupré, B. Fournier, O. Gondel, M. Riou, J. Isaac, Pascal Garrec, B. Vi-Fane, Samia Kribel, M. de La Dure-Molla, M. Carra, R. Felizardo, S. Kerner   +11 more
semanticscholar   +1 more source

Abstract 13325: Novel Heterozygous EFEMP2 Variant Detected in a Patient With Bilateral Internal Carotid Artery Dissection and Oligodontia

Circulation, 2023
Cutis laxa is a rare connective tissue disorder characterized by sagging or inelastic skin. This phenotype is caused by multiple genotype variants. Biallelic variants in the EFEMP2 gene cause cutis laxa subtype IB characterized by aortic aneurysm ...
Olivia Millay, Mary Sheppard, Liisa Bergmann, James Hartsfield   +3 more
semanticscholar   +1 more source

WNT10A mutations causing oligodontia

Archives of Oral Biology, 2019
To identify the molecular genetic etiology of the families with non-syndromic multiple missing permanent teeth (oligodontia).Genomic DNA was isolated and measured, and whole-exome sequencing was performed. The obtained sequencing reads were aligned to the human reference genome and subsequently processed by a series of bioinformatics programs. Finally,
Haemin, Park, Ji-Soo, Song, Teo Jeon, Shin, Hong-Keun, Hyun, Young-Jae, Kim, Jung-Wook, Kim   +5 more
openaire   +2 more sources

Oligodontia in pseudoxanthoma elasticum

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2007
Pseudoxanthoma elasticum (PXE) is an inherited disorder that has both autosomal recessive and autosomal dominant pathways and is characterized by severe malformation of elastic and collagen fibers. Clinically, 3 main groups of systemic findings involving skin, eye, and vessels emerge in the symptoms.
Sayin, M. Ozgur, Ozen, Tuncer, Esenlik, Elcin, Karahan, Nermin, Atilla, A. Onur   +4 more
openaire   +3 more sources

Oligodontia: a case report

Journal of Clinical Pediatric Dentistry, 2001
Oligodontia is the agenesis of numerous teeth, and is commonly associated with specific syndromes and / or severe systemic abnormalities. In this paper a patient with 14 missing permanent teeth is presented clinically with her conservative and prosthetic treatments.
F, Unalan, I, Ulukapi, J, Bakirgil
openaire   +2 more sources