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Management of Osteogenesis Imperfecta
Osteogenesis imperfecta (OI) is the term used to describe a group of rare inherited skeletal disorders characterized by a greatly increased risk of fragility fractures (1). Mutations in several genes can cause OI but the condition is most commonly caused by mutations of COLIA1 or COL1A2 resulting in...
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| Published in: | Front Endocrinol (Lausanne) |
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| Main Authors: | , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Frontiers Media S.A.
2020
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7026366/ https://ncbi.nlm.nih.gov/pubmed/32117044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2019.00924 |
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