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Osteogenesis imperfecta and dentinogenesis imperfecta: Associated disorders
(Quintessence Publ Co IncCarol StreamEUA, 2005)
The role of dentists in-diagnosing osteogenesis imperfecta in patients with dentinogenesis imperfecta
(AMER DENTAL ASSOC, 2008)
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult to diagnose in its mild form. The authors describe a clinical case of a diagnosis of dentinogenesis imperfecta (DI), In ...
Dentinogénesis imperfecta: reporte de un casoDentinogénesis imperfecta: reporte de un caso
(Facultad de Odontología, 2010)
Dentinogenesis imperfecta type II: approach for dental treatment
(Universidade Estadual Paulista Júlio de Mesquita Filho, 2012-12-01)
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affects both primary and permanent dentitions. The DI characteristics are discolored and translucent teeth ranging from gray to ...
Dentinogenesis imperfecta: a case report of five patients in the same family group
(Facultad de Ciencias, 2016)
La dentinogénesis imperfecta (DI) es un tipo de displasia de la dentina que afecta su estructura en una o ambas denticiones. La DI puede clasificarse en tres tipos. El objetivo de este informe fue demostrar las características ...
A novel COL1A1 gene-splicing mutation (c. 1875+1G > C) in a Brazilian patient with osteogenesis imperfecta
(FUNPEC-EDITORA, 2009)
Osteogenesis imperfecta is a heterogeneous genetic disorder characterized by bone fragility and deformity, recurrent fractures, blue sclera, short stature, and dentinogenesis imperfecta. Most cases are caused by mutations ...