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Resin Infiltration: Ultraconservative Treatment Options for Carious and Non-carious Enamel Lesions
Purpose of ReviewOriginally developed for the noninvasive treatment of incipient proximal caries lesions, resin infiltration has gained popularity...
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Orthodontic findings and treatment need in patients with amelogenesis imperfecta: a descriptive analysis
Introduction: Amelogenesis imperfecta (AI) is a genetically determined, non-syndromic enamel dysplasia that may manifest as hypoplasia,...
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Restorative treatment in a case of amelogenesis imperfecta and 9-year follow-up: a case report
BackgroundAmelogenesis imperfecta is a hereditary malformation showing various manifestations regarding enamel dysplasia. This case report shows a...
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Comparative evaluation of effect of chlorhexidine application on dentin bond strength with two different adhesives after ER, CR: YSGG phototherapy: an in vitro study
This study aimed to assess the efficacy of phototherapy with an Er, Cr:YSGG laser on the bond strength of dentin using two different adhesive systems...
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Management guidelines for amelogenesis imperfecta: a case report and review of the literature
BackgroundRehabilitation of the entire dentition with amelogenesis imperfecta (AI) tends to pose a great challenge to the clinician. Most of the...
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Long-Term Effect of Anticancer Therapy on Dentition in Childhood Cancer Survivors: An Observational, Cross-Sectional Study
ObjectivesTo evaluate the presence of developmental dental anomalies, like microdontia, hypodontia, abnormally shaped teeth (AST), and developmental...
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Oculo-facio-cardio-dental (OFCD) syndrome: a case report
BackgroundOculo-facio-cardio-dental (OFCD) syndrome is a rare condition that affects the eyes, face, heart, and teeth of patients. One notable dental...
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A pictorial review of the radiographic skeletal findings in Morquio syndrome (mucopolysaccharidosis type IV)
Morquio syndrome, also known as Morquio-Brailsford syndrome or mucopolysaccharidosis type IV (MPS IV), is a subgroup of mucopolysaccharidosis. It is...
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Deep neurological phenoty** in oculo-dento-digital syndrome
ObjectivesOculodentodigital dysplasia (ODDD) is a rare autosomal dominant congenital malformation syndrome characterized by high penetrance and great...
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Rethinking the Genetic Etiology of Nonsyndromic Tooth Agenesis
Purpose of ReviewGenetic studies in humans and animal models have improved our understanding of the role of numerous genes in the etiology of...
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Investigating the correlation between genotype and phenotype in Prader-Willi syndrome: a study of 45 cases from Brazil
BackgroundPrader-Willi syndrome (PWS) is a genetic disorder characterized by abnormalities in the 15q11-q13 region. Understanding the correlation...
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Phenotypic variability in distal acidification defects associated with WDR72 mutations
BackgroundDistal renal tubular acidosis (RTA) is typically caused by defects in ATP6V0A4 , ATP6V1B1 , and SLC4A1 , accounting for 60–80% of patients . ...
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Potential Risks of Corneal Refractive Surgery in Patients with Ectodermal Dysplasia
Ectodermal dysplasia (ED) involves the aberrant development of at least two ectodermal derivatives, such as skin, teeth, hair, sweat glands, and...
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The association between low birth weight and dental caries among 11-to-13-year-old school age children in Ningbo, China
BackgroundThe association between low birth weight (LBW) and dental caries is currently unclear. The aim of this study was to investigate the...
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Craniofacial syndromes and class III phenotype: common genotype fingerprints? A sco** review and meta-analysis
AbstractSkeletal Class III (SCIII) is among the most challenging craniofacial dysmorphologies to treat. There is, however, a knowledge gap regarding...
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Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia
Adrenal insufficiency (AI) is a severe endocrine disorder characterized by insufficient glucocorticoid (GC) and/or mineralocorticoid (MC) secretion...
