Clinical Aspects, Imaging Features, and Considerations on Bisphosphonate-Related Osteonecrosis Risk in a Pediatric Patient with Osteogenesis Imperfecta

Osteogenesis imperfecta (OI) is a rare hereditary condition caused by changes in collagen metabolism. It is classified into four types according to clinical, genetic, and radiological criteria. Clinically, bone fragility, short stature, blue sclerae, and locomotion difficulties may be observed in th...

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Detalles Bibliográficos
Autores principales: Costa, Fábio Wildson Gurgel, Chaves, Filipe Nobre, Nogueira, Alexandre Simões, Rodrigues Carvalho, Francisco Samuel, Pereira, Karuza Maria Alves, Kurita, Lúcio Mitsuo, Rodrigues, Rodrigo Rodrigues, Fonteles, Cristiane Sá Roriz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158459/
https://www.ncbi.nlm.nih.gov/pubmed/25215248
http://dx.doi.org/10.1155/2014/384292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158459/
https://www.ncbi.nlm.nih.gov/pubmed/25215248
http://dx.doi.org/10.1155/2014/384292

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