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Osteogenesis Imperfecta (Type IV) with Dental Findings in Siblings
Osteogenesis imperfecta (OI) is a hereditary disorder characterized by increased tendency for bone fractures due to high fragility. The clinical and radiological features of OI manifest in different age groups, although the disease is congenital in nature. Besides bone fragility, features like laxit...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Hindawi Publishing Corporation
2011
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3335498/ https://ncbi.nlm.nih.gov/pubmed/22567450 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/970904 |
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