Custom hemiarthroplasties for retention of existing hardware associated with osteogenesis imperfecta

Osteogenesis imperfecta is a rare genetic disorder that presents with heterogeneous phenotypes ranging from brittle bones to impaired hearing. Because of the decreased bone mineral density frequently observed in this patient population, many patients experience recurring and long-term fractures, whi...

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Detalles Bibliográficos
Autores principales: Nishida, Kevin, Choi, Daniel, Bostrom, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485223/
https://www.ncbi.nlm.nih.gov/pubmed/28695180
http://dx.doi.org/10.1016/j.artd.2017.01.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485223/
https://www.ncbi.nlm.nih.gov/pubmed/28695180
http://dx.doi.org/10.1016/j.artd.2017.01.004

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