Results 61 to 70 of about 10,573 (205)
Prenatal ultrasound and postmortem histologic evaluation of tooth germs: an observational, transversal study [PDF]
Introduction: Hypodontia is the most frequent developmental anomaly of the orofacial complex, and its detection in prenatal ultrasound may indicate the presence of congenital malformations, genetic syndromes and chromosomal abnormalities.To date, only a ...
A Kapdan +33 more
core +2 more sources
ABSTRACT Background/Aims To evaluate the prevalence and timing of post‐operative complications following tooth autotransplantation, identify factors associated with earlier diagnosis, and report long‐term survival and success rates. Materials and Methods A single‐centre retrospective cohort study was conducted at a Czech university dental clinic (2003 ...
Juraj Marton +5 more
wiley +1 more source
Agenesis of teeth in a patient who also presents with a supernumerary tooth is one of the rare numerical anomalies in human dentition. Agenesis of third molars was shown to be associated with other missing permanent teeth.
Sivakumar Nuvvula +3 more
doaj +1 more source
Waardenburg syndrome type I: dental phenotypes and genetic analysis of an extended family [PDF]
Background: The aim of this study was to describe the pattern of inheritance and the clinical features in a large family with Waardenburg syndrome type I (WS1), detailing the dental abnormalities and screening for PAX3 mutations ...
Aquino, Sibele Nascimento de +8 more
core +1 more source
ABSTRACT Objectives This study aimed to investigate the relationship between functional independence, oral hygiene habits and periodontal status in patients with Down syndrome (DS). Methods A cross‐sectional observational study was conducted with 49 patients with Down Syndrome. Sociodemographic data, oral hygiene habits and functional independence were
Joana Albuquerque Bastos de Sousa +6 more
wiley +1 more source
Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis. [PDF]
Congenital tooth agenesis in human is characterized by failure of tooth development during tooth organogenesis. 300 genes in mouse and 30 genes in human so far have been known to regulate tooth development. However, candidature of only 5 genes viz. PAX9,
Tanmoy Sarkar +2 more
doaj +1 more source
The acrocallosal syndrome: A case report and literature survey [PDF]
Acrocallosal syndrome (ACS) is a rare, genetically transmitted disorder characterized by facial deformities. These include a large forehead, large anterior fontanelle, broad nasal bridge with increased intercanthal distance, partial or complete agenesis ...
Davies, Lindsey +2 more
core +1 more source
ABSTRACT Objective To evaluate the impact of lithium disilicate cantilever resin‐bonded fixed dental prostheses (RBFDPs) on oral health‐related quality of life (OHRQoL), patient satisfaction, and esthetic outcomes in patients with a missing maxillary incisor.
Joyce A. Jonker +3 more
wiley +1 more source
MSX1 variant causes nonsyndromic tooth agenesis in a Japanese patient
MSX1 variants are associated with autosomal dominant craniofacial developmental anomalies, including congenital tooth agenesis. Here, whole-exome sequencing in a Japanese patient with congenital tooth agenesis identified a novel de novo heterozygous ...
Yasuto Sano +7 more
doaj +1 more source
A review of implant provision for hypodontia patients within a Scottish referral centre [PDF]
Background: Implant treatment to replace congenitally missing teeth often involves multidisciplinary input in a secondary care environment. High quality patient care requires an in-depth knowledge of treatment requirements.
A Dasmah +21 more
core +1 more source

