نتایج جستجو برای: dentinogenesis imperfecta

تعداد نتایج: 5063  

Journal: :Acta of bioengineering and biomechanics 2013
Aneta Wieczorek Jolanta Loster Wojciech Ryniewicz Anna M Ryniewicz

Dentinogenesis imperfecta type II (DI-II) is the most common dental genetic disease with reported incidence 1 in 8000. Elasticity and hardness of the enamel of teeth are important values which are connected with their resistance to attrition. It is hypothesized that values of physical properties for healthy teeth and teeth with DI-II are different. The aim of the study was to investigate some p...

Journal: :Applied sciences 2022

Universal nanofilled adhesives were recently introduced in restorative dentistry to simplify clinical procedures and improve adhesion different situation. This study investigated the effectiveness of two universal on both sound dentinogenesis imperfecta type II (DI-II)-affected teeth. To evaluate DI-II-affected teeth, four samples, extracted molars affected by DI-II selected. Coronal enamel den...

Journal: :Orphanet Journal of Rare Diseases 2008
Martin J Barron Sinead T McDonnell Iain MacKie Michael J Dixon

The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000, whereas that of DD type 1 is 1 in 100,000. Clinically, the t...

مروتی, سعید, ناصری, فرنوش,

Dentinogenesis imperfecta (DI) is an inherited disorder affecting dentin. Defective dentin formation results in discolored teeth that are prone to attrition and fracture. Mutation in dentin and the main gene in this disease is DSPP. Heterozygous mutations in this gene cause tooth sialophosphoprotein (DSPP) causes dentin disorders DI I and II. Imperfecta is a dominant autosomal trait that affec...

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