ss Open AcceReview Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia Martin J Barron1, Sinead T McDonnell2, Iain MacKie2 and Michael J Dixon*1,2

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art14Marco A. Bolaños E. * Key Word Index: Dentinogénesis imperfecta. RESUMEN Se presenta un caso de dentinogénesis imperfecta en un paciente de 4 años

RESEARCH ARTICLE Open Access A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family Haihua Bai1,2, Hasi Agula1, Qizhu Wu2, Wenyu Zhou3,

192 GACETA DENTAL 190, marzo 2008 INTRODUCCIÓN La osteogénesis imperfecta (OI) es una enfermedad grave cuyo rasgo principal es la fragilidad ósea. Esta

untitledORIGINAL INVESTIGATION J.-W. Kim . S.-H. Nam . K.-T. Jang . S.-H. Lee . C.-C. Kim . S.-H. Hahn . J. C.-C. Hu . J. P. Simmer A novel splice acceptor mutation in the

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Living with OI:Serving the OI community with information and support since 1970 Dental Care for People with Osteogenesis Imperfecta Introduction Osteogenesis imperfecta (OI)

Vol15 No2.inddImperfecta Dentinogenesis: a case report Patricia TREJOS1, Vanessa HERNANDO2, Claudia S. DE LEóN3 1. Profesor de la Especialidad de Odontopediatría.