نتایج جستجو برای: dentinogenesis imperfecta
تعداد نتایج: 5063 فیلتر نتایج به سال:
A large family from a small village in Madagascar, Antanetilava, is known to present with colored teeth. Through previous collaboration and 4 successive visits in 1994, 2004, 2005, and 2012, we provided dental care to the inhabitants and diagnosed dentinogenesis imperfecta. Recently, using whole exome sequencing we confirmed the clinical diagnosis by identifying a novel single nucleotide deleti...
Dentinogenesis imperfecta type II or hereditary opalscent dentin is one of the most common autosomal dominant anomaly of dentin that occurs in both sex affecting approximately 1:8000 persons. Clinically this disorder is characterized by variable blue gray to yellow brown teeth, with fracture of enamel and excessive wear. The treatment strategy is focused towards protecting teeth from further we...
ACKNOWLEDGEMENTS During this work, the first author was supported by the National Health and Medical Research Council of Australia Public Health Postdoctoral Fellowship Number 997096 and National Health and Medical Research Council of Australia Travelling Fellowship Grant ID 235610. This paper is one of a series of short papers on aspects of research by Linda Shields and Alison Twycross The fir...
Osteogenesis imperfecta (OI) is a hereditary bone fragility disorder that in most patients is caused by mutations affecting collagen type I. Their typical oral and craneofacial characteristics (Dentinogenesis imperfecta type I and class III malocclusion), involve the dentist in the multidisciplinary team that treat these patients. It is usual to perform lateral skull radiographs for the orthodo...
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