Results 51 to 60 of about 127,214 (299)
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
OBJECTIVES We present a new distance-based exponential regression approach based on published histological data to refine the objectivity, accuracy, and precision of age estimates of LEH defect formation on the anterior dentition.
Alejandra Cares Henriquez, M. Oxenham
semanticscholar +1 more source
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
Enamel hypoplasia in a Mesolithic (5900±100 BC) individual from Woźna Wieś (Poland): a case study
Modern anthropological research includes very sophisticated diagnostic methods. They allow us to obtain information that has not been available so far.
Tomczyk Jacek, Ostrowska Agnieszka
doaj +1 more source
Enamel Hypoplasia Related to Historical Famine Stress in the Contemporary Chinese Population
Linear enamel hypoplasia (LEH), a defect in enamel formation, has been frequently attributed to malnutrition and other physiological stress during periods of enamel development (Sarnat and Schour, 1941; Kreshover, 1960).
Liming Zhou, Robert S. Corruccini
doaj +1 more source
Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations [PDF]
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
The role of Rho GTPases in facial morphogenesis
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
Apeced in Turkey: a case report and insights on genetic and phenotypic variability [PDF]
APECED is a rare monogenic recessive disorder caused by mutations in the AIRE gene. In this manuscript, we report a male Turkish patient with APECED syndrome who presented with chronic mucocutaneous candidiasis associated with other autoimmune ...
Alessandra Fierabraccia +4 more
core +1 more source
Enamel hypoplasia of primary canine: Its prevalence and degree of expression
Background: Enamel hypoplasia is a unique lesion showing wide variations in prevalence among populations. The present study aimed to evaluate frequency and degree of expression of enamel hypoplasia of primary canine in populations living in the eastern ...
Santanu Mukhopadhyay +4 more
openalex +2 more sources
Reduced Dietary Protein Induces Changes in the Dental Proteome
Low dietary protein (10%) from normal (20%) does change protein expression in tooth proteome and alter developmental pathways. Among the significant protein expressions changes are actin‐based myosins, tooth, and bone development proteins. Perplexingly tooth size is not altered, suggesting more nuanced phenotypic response to low dietary protein in ...
Robert W. Burroughs +2 more
wiley +1 more source

