Results 61 to 70 of about 8,907 (247)
Non-syndromic hypodontia (NSH) in permanent teeth – epidemiological study [PDF]
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
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]
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
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]
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
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
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]
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
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]
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