Results 61 to 70 of about 37,360 (271)

DENTAL ENAMEL HYPOPLASIA: literature review

open access: yes, 2022
Enamel hypoplasias are problems caused by both endogenous and exogenous factors during the process of tooth enamel development, the structures affected by these aggressive agents are the enamel secreting cells and ameloblasts. Hypoplasias can be clinically characterized from mild white spots noticeable only during close clinical examinations to ...
Paulo, Moises Lucio de   +1 more
openaire   +1 more source

Prevalence and Treatment Need of Molar Incisor Hypomineralisation in 8-12 Year Old School Going Children of Cuttack, Odisha [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2020
Introduction: Molar Incisor Hypomineralisation (MIH) is a condition where one or more first permanent molars with or without permanent incisors are hypomineralised due to disturbances during the maturation phase.
Prayas Ray   +4 more
doaj   +1 more source

The Effects of Urban Living on Child, Infant, and Maternal Health: A Comparative Study of Linear Enamel Hypoplasia Between Two Dutch Postmedieval Populations

open access: yesInternational Journal of Osteoarchaeology
Substantial research has been done assessing health inequalities between rural and urban contexts in the low countries; however, fewer studies have considered the effect of urban living on non‐adults. Because dental enamel does not remodel, recording the
Oriana Chiappa, S. Schrader
semanticscholar   +1 more source

Family's socioeconomic and demographic factors on elements of children's dental and oral health: A scoping review

open access: yesClinical and Experimental Dental Research, EarlyView.
Abstract Background Family plays a significant role in children's dental and oral health (DOH) elements, such as children's DOH knowledge and practice, the development of children's dental fear and anxiety (DFA), children's dental visits, and children's DOH status.
Wisnu Fadila   +5 more
wiley   +1 more source

A Longitudinal Study of Streptococcus mutans Colonization in Infants after Tooth Eruption [PDF]

open access: yes, 2003
We previously reported that, before tooth eruption, over one-half of infants aged 6 mos were already infected with Streptococcus mutans. The aim of this investigation was to determine the colonization of S.
Bird, P. S.   +5 more
core   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki   +6 more
wiley   +1 more source

The effect of fluoride on enamel and dentin formation in the uremic rat incisor [PDF]

open access: yes, 2008
Renal impairment in children is associated with tooth defects that include enamel pitting and hypoplasia. However, the specific effects of uremia on tooth formation are not known.
A Al Nowaiser   +28 more
core   +1 more source

The role of Rho GTPases in facial morphogenesis

open access: yesDevelopmental Dynamics, EarlyView.
The role of small GTPases, RHOA, RAC1, and CDC42 and pathway mediators is reviewed in the context of embryonic facial development. Lip fusion requires cytoskeletal remodeling during morphogenesis of the facial processes and during lip fusion. Fnm, frontonasal mass; lnp, lateral nasal process; mnp, medial nasal process; mxp, maxillary process; np, nasal
Isra Ibrahim, Joy M. Richman
wiley   +1 more source

Prenatal and Early Childhood Determinants of Enamel Hypoplasia in Infants

open access: yes, 2021
Objective: Enamel hypoplasia (EH) is a recognized risk factor for dental caries. The purpose was to investigate the relationship between prenatal and early life risk factors, including prenatal nutritional status, and EH among infants.
Schroth Rj   +3 more
semanticscholar   +1 more source

Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations [PDF]

open access: yes, 2015
Background: Raine syndrome (RS) is a rare autosomal recessive bone dysplasia typified by osteosclerosis and dysmorphic facies due to FAM20C mutations. Initially reported as lethal in infancy, survival is possible into adulthood. We describe the molecular
A Linde   +61 more
core   +2 more sources

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