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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Bibliographic Details
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
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Online Access:https://doi.org/10.1186/s13023-024-03452-y
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