Lung function in adult patients with osteogenesis imperfecta: a cohort study
Abstract Background Osteogenesis imperfecta (OI) is a rare hereditary bone disease resulting from a defect in collagen synthesis or processing, leading to bone fragility, frequent fractures and skeletal deformities. OI is associated with increased respiratory morbidity and mortality, but the mechani...
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| Main Authors: | Alexandra Lenoir, Bérengère Aubry-Rozier, Aline Bregou, Elena Gonzalez Rodriguez, Célia Paquier, Joëlle Tanniger, Mohamed Faouzi, Romain Lazor |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2024-12-01
|
| Series: | Orphanet Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13023-024-03452-y |
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