Results 61 to 70 of about 8,907 (247)

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

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

Familial cases of missing mandibular incisor: three case presentations [PDF]

open access: yes, 1999
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  

Hypodontia Patterns and Natural Dental Compensation Movements. An Orthopantomographic Study

open access: yesRomanian Journal of Oral Rehabilitation, 2012
The study aims to detect on orthopantomogram the hypodontia of permanent teeth, setting the hypodontia frequency patterns for each patient and on both sexes and their correlation.
Georgeta Zegan   +3 more
doaj  

Removable Partial Dentures vs Overdentures in Children with Ectodermal Dysplasia: Two Case Reports [PDF]

open access: yes, 2016
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

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

Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients

open access: yesClinical Genetics, Volume 108, Issue 3, Page 334-346, September 2025.
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut   +7 more
wiley   +1 more source

Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis. [PDF]

open access: yes, 2009
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

Development and assessment of reliable patient-based hypodontia website

open access: yesPatient Preference and Adherence, 2018
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  

Oral characteristics of Trisomy 8 and monosomy 18: a case report [PDF]

open access: yes, 2011
Several reports described various mosaic chromosomal syndromes characterized by alterations originated by either an excess or deficit in the number of chromosomes.
Campus, Guglielmo Giuseppe   +3 more
core   +1 more source

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