Osteogenesis imperfecta and clubfoot—a rare combination: Case report and review of the literature

BACKGROUND: Osteogenesis imperfecta (OI) is a rare congenital genetic osteodystrophy, which has a prevalence of 1:20,000. OI is caused by the mutation of the COL1A1/COL1A2 genes, leading to a deficit of quality and/or quantity in the synthesis of procollagen-α type 1. Seven different forms of divers...

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Detalles Bibliográficos
Autores principales: Persiani, Pietro, Ranaldi, Filippo Maria, Martini, Lorena, Zambrano, Anna, Celli, Mauro, D’Eufemia, Patrizia, Villani, Ciro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979856/
https://www.ncbi.nlm.nih.gov/pubmed/27495102
http://dx.doi.org/10.1097/MD.0000000000004505

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979856/
https://www.ncbi.nlm.nih.gov/pubmed/27495102
http://dx.doi.org/10.1097/MD.0000000000004505

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