Dental anomalies in individuals with osteogenesis imperfecta: a systematic review and meta-analysis of prevalence and comparative studies

BACKGROUND: Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease. OBJECTIVE: This study aims to describe the prevalence of dental anomalies (except dentinogenesis imp...

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Detalles Bibliográficos
Autores principales: PRADO, Heloisa Vieira, SOARES, Enio Cássio Barreto, CARNEIRO, Natália Cristina Ruy, VILAR, Ivanete Cláudia de Oliveira, ABREU, Lucas Guimarães, BORGES-OLIVEIRA, Ana Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculdade De Odontologia De Bauru - USP 2023
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506791/
https://www.ncbi.nlm.nih.gov/pubmed/37672427
http://dx.doi.org/10.1590/1678-7757-2023-0040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506791/
https://www.ncbi.nlm.nih.gov/pubmed/37672427
http://dx.doi.org/10.1590/1678-7757-2023-0040

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