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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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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4979856/ https://ncbi.nlm.nih.gov/pubmed/27495102 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000004505 |
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