Results 11 to 20 of about 13,585 (261)

EVALUATION OF DENTAL ANOMALY PREVELANCE AND TYPES BY CONE BEAM COMPUTED TOMOGRAPHY IN A SUBGROUP OF TURKISH POPULATİON [PDF]

open access: yesJournal of Oral Health and Oral Epidemiology
Background: This study aimed to investigate the frequency and variation of dental malformations in a subgroup of the Turkish population.Methods: Cone beam computed tomography (CBCT) images taken for various reasons were scanned retrospectively.
Rumeysa Sendisci GOK   +1 more
doaj   +1 more source

Prevalence of dental anomalies in cleft lip and palate patients

open access: yesInternational Dental Journal, 2021
Aim or Purpose: The study was performed to investigate the prevalence of dental anomalies in Moroccan patients with cleft lip and palate. Materials and Methods: Ninety-six cleft patients referring to the dental care center of Casablanca (CCTD) and the ...
Soukaina Sahim   +3 more
doaj   +1 more source

Prevalence and Distribution of Dental Anomalies among Arab Orthodontic Patients in Israel: Is There a Correlation to Consanguinity Marriage?

open access: yesApplied Sciences, 2022
The aim of this study was to determine the prevalence of dental anomalies and whethera significant association exists between dental anomalies and consanguinity marriage among Arabic orthodontic patients in Israel.
Rana Kadry   +6 more
doaj   +1 more source

Prevalence and distribution of selected developmental dental anomalies in Taif, Saudi population

open access: yesJournal of Public Health Research, 2021
Background: Developmental dental anomalies are seen as abnormalities in tooth size, shape, position, and structure due to multiple reasons during various stages of tooth development.
Theeb Saed Saad Aljuaid   +5 more
doaj   +1 more source

Hyperdontia: Exploring the Developmental Abnormality

open access: yesJournal of Pre-Clinical and Clinical Research, 2020
Introduction and objective Hyperdontia is a dental developmental anomaly in which supernumerary teeth exist. These are extra teeth to the normal set of primary or permanent dentitions.
Naji Ziad Arandi
doaj   +1 more source

Prevalence of dental anomalies in a Mexican population

open access: yesDentistry 3000, 2014
Background: Data on dental anomaly prevalence is instrumental to diagnosis and treatment in different populations. A retrospective study was done to determine dental anomaly prevalence and associations in a group of orthodontic patients in a Mexican ...
Jose Ruben Herrera-Atoche   +4 more
doaj   +1 more source

TFAP2B mutation and dental anomalies [PDF]

open access: yesJournal of Human Genetics, 2017
Mutations inTFAP2B has been reported in patients with isolated patent ductus arteriosus (PDA) and Char syndrome. We performed mutation analysis of TFAP2B in 43 patients with isolated PDA, 7 patients with PDA with other congenital heart defects and 286 patients with isolated tooth agenesis with or without other dental anomalies. The heterozygous c.1006G>
Tanasubsinn, Natchaya   +7 more
openaire   +2 more sources

Bilateral radicular dens in dente in mandibular premolars

open access: yesJournal of Oral and Maxillofacial Radiology, 2013
Dens invaginatus (DI) is a rare developmental anomaly that results from an invagination of the enamel organ into the dental papilla during odontogenesis.
Kanika Gupta Verma   +3 more
doaj   +1 more source

Exploring the Association Between Genetic Polymorphisms in Genes Involved in Craniofacial Development and Isolated Tooth Agenesis

open access: yesFrontiers in Physiology, 2021
Tooth agenesis is a common congenital anomaly in humans and is more common in oral cleft patients than in the general population. Many previous studies suggested that oral cleft and tooth agenesis share a similar genetic background. Therefore, this study
Erika Calvano Küchler   +10 more
doaj   +1 more source

Complex Microphthalmia due to a Homozygous Novel Variant in SIX Homeobox 6 Gene

open access: yesDelhi Journal of Ophthalmology, 2023
Microphthalmia is an ocular anomaly with wide genetic heterogeneity. Many monogenic causes have been identified recently by next-generation sequencing. Here, we describe the genotype and phenotype of two siblings with complex microphthalmia. The siblings
Mayank Nilay, Amita Moirangthem
doaj   +1 more source

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