Results 31 to 40 of about 3,873 (165)

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

Non-syndromic hypodontia (NSH) in permanent teeth – epidemiological study [PDF]

open access: yesRomanian Journal of Stomatology, 2020
Aim. Assessment of characteristics of non-syndromic hypodontia (NSH) in permanent teeth (PT) in a group of Romanian children and adolescents. Material and method. Descriptive retrospective observational study on dental files and orthopantomograms of 138
Ioana-Andreea Stanciu   +5 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

Non‐Isolated Dandy‐Walker Malformation: Exome Sequencing Efficacy and Phenotypic Expansions

open access: yesClinical Genetics, EarlyView.
Exome sequencing identified a diagnosis in 35% of 91 individuals with non‐isolated Dandy Walker malformation (DWM+). Only 24%–55% of these diagnoses could be made using a gene panel. We then demonstrated that DWM is a feature of disorders associated with ANKRD11, C2CD3, COL4A1, KMT2D, KRAS, OPHN1, SHOC2, SMARCB1, and WDR73.
Sarah Araji   +4 more
wiley   +1 more source

Stapled side‐to‐side anastomosis to treat a pelvic flexure stricture in a miniature horse

open access: yesEquine Veterinary Education, EarlyView.
Summary Fecaliths are a recognised cause of non‐strangulating colon obstruction in horses. Although they more commonly obstruct the small colon, they can also lodge in the pelvic flexure, requiring enterotomy for removal. Stricture at the enterotomy site is an uncommon but surgically significant complication.
M. Baglioni   +5 more
wiley   +1 more source

A multidisciplinary approach for the management of hypodontia: case report

open access: yesJournal 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   +6 more
doaj   +1 more source

Ketone Utilization Disorder and Hypodontia

open access: yesThe Journal of Pediatric Research, 2015
Hypodontia is defined as the congenital missing of one or more teeth in one or both dentition periods. In this case report, ketone utilization disorder with oro-dental findings was reported which was previously not reported in the literature. It was concluded that dental examination is an important parameter which must be taken into consideration in ...
Alacam, Alev   +2 more
openaire   +4 more sources

Optimizing Hard and Soft‐Tissue Esthetics With Anterior Cantilever Zirconia Ceramic Resin‐Bonded Fixed Dental Prostheses

open access: yesJournal of Esthetic and Restorative Dentistry, EarlyView.
ABSTRACT Objective The replacement of missing maxillary lateral incisors poses both functional and esthetic challenges, not only from a restorative but also from a periodontal aspect. This case report presents a step‐by‐step protocol for ideal hard and soft‐tissue esthetics with cantilever zirconia ceramic resin‐bonded fixed dental prostheses (RBFDPs).
Markus B. Blatz   +3 more
wiley   +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

open access: yesProgress 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   +7 more
doaj   +1 more source

Identification of copy neutral loss of heterozygosity on chromosomes 1p, 1q, and 6p among nonsyndromic cleft lip and/or without cleft palate with hypodontia

open access: yesBMC Oral Health, 2023
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

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