Results 31 to 40 of about 12,368 (291)
Differential Expression of Hard Tissue Proteins in Hypomineralized Second Primary Molars in Comparison to Normal Teeth. [PDF]
Clin Exp Dent ResABSTRACT Objective This study aims to identify the proteins in hypomineralized second primary molars (HSPMs) and correlate their function in Amelogenesis. HSPM is a qualitative defect of the enamel of the second primary molars with no clear etiology.
Jessica S +9 more
europepmc +2 more sources
Clear Aligners in Patients with Amelogenesis and Dentinogenesis Imperfecta
International Journal of Dentistry, 2021 Dentinogenesis imperfecta (DI) and amelogenesis imperfecta (AI) are hereditary abnormalities of dental hard tissues. Dental abnormalities may also be accompanied by symptoms of disorders such as osteogenesis imperfecta.
Nozha M Sawan
semanticscholar +1 more source
Restorative Treatment of Amelogenesis Imperfecta with Prefabricated Composite Veneers
Case Reports in Dentistry, 2021 This case report presents the use of prefabricated composite veneers for restorative treatment of amelogenesis imperfecta (AI). This technique bridges the gap between a conventional direct technique and a conventional indirect technique and introduces an
C. Novelli, M. Pascadopoli, A. Scribante
semanticscholar +1 more source
Frontiers in Pharmacology, 2021 Background: Amelogenesis, the formation of dental enamel, is well understood at the histomorphological level but the underlying molecular mechanisms are poorly characterized.
Anna Földes +8 more
doaj +1 more source
A Novel De Novo SP6 Mutation Causes Severe Hypoplastic Amelogenesis Imperfecta
Genes, 2021 Amelogenesis imperfecta (AI) is a heterogeneous group of rare genetic disorders affecting tooth enamel formation. Here we report an identification of a novel de novo missense mutation [c.817_818delinsAT, p.(Ala273Met)] in the SP6 gene, causing non ...
Y. J. Kim +6 more
semanticscholar +1 more source
Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta
Journal of Personalized Medicine, 2021 Amelogenesis imperfecta (AI) is a rare genetic condition affecting the quantity and/or quality of tooth enamel. Hypomaturation AI is characterized by brownish-yellow discoloration with increased opacity and poorly mineralized enamel prone to fracture and
F. Seymen +6 more
semanticscholar +1 more source
Molar incisor hypomineralisation: current knowledge and practice
International Dental Journal, EarlyView., 2020 Background Molar incisor hypomineralisation (MIH) is a common developmental dental condition that presents in childhood. Areas of poorly formed enamel affect one or more first permanent molars and can cause opacities on the anterior teeth. MIH presents a variety of challenges for the dental team as well as functional and social impacts for affected ...
Helen D. Rodd +4 more
wiley +1 more source
Amelogenesis imperfecta. Case report
Revista Científica Odontológica, 2023 The main origin of amelogenesis imperfecta (AI) is a genetic alteration inherited by a family member which affects the dental enamel of the teeth of a person with this condition in various ways. The present clinical case from the Teaching Dental Clinic of the Peruvian University Cayetano Heredia is of a 6-year 5-month-old male child who came to the ...
Nicole Alessandra Herrera-Rojas +1 more
openaire +3 more sources
Significance of pH cyclization in amelogenesis
Fogorvosi Szemle, 2021 The process of amelogenesis is well understood at the histomorphological level, but the regulation of crystal formation and the underlying molecular mechanisms are still largely unknown.
Róbert Rácz +4 more
doaj +1 more source
International Journal of Molecular Sciences, 2021 Amelogenesis imperfecta is a congenital form of enamel hypoplasia. Although a number of genetic mutations have been reported in humans, the regulatory network of these genes remains mostly unclear.
Hiroki Yoshioka +6 more
semanticscholar +1 more source