Cargando…
Dentinogenesis imperfecta type II: A case report with 17 years of follow-up
Dentinogenesis imperfecta is a dominant autosomal hereditary disorder of dentin formation that affects the deciduous and permanent teeth. Its etiology is characterized by inadequate cell differentiation during odontogenesis. The clinical characteristics of dentinogenesis imperfecta are discolored te...
Autores principales: | Gama, Francisco José Reis, Corrêa, Isabella Sousa, Valerio, Claudia Scigliano, Ferreira, Emanuelle de Fátima, Manzi, Flávio Ricardo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Oral and Maxillofacial Radiology
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489669/ https://www.ncbi.nlm.nih.gov/pubmed/28680850 http://dx.doi.org/10.5624/isd.2017.47.2.129 |
Ejemplares similares
-
Dentinogenesis imperfecta associated with osteogenesis imperfecta
por: Biria, Mina, et al.
Publicado: (2012) -
Prosthodontic rehabilitation of dentinogenesis imperfecta
por: Goud, Anil, et al.
Publicado: (2011) -
Dentinogenesis imperfecta type II in Swedish children and adolescents
por: Andersson, K., et al.
Publicado: (2018) -
Phenotypic Properties of Collagen in Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta
por: Ibrahim, Salwa, et al.
Publicado: (2019) -
Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children
por: Nguyen, Huong Thi Thu, et al.
Publicado: (2021)