Osteogenesis Imperfecta Type 3 in a 10-Year-Old Child With Acute Respiratory Distress Syndrome

Osteogenesis imperfecta (OI) represents a group of rare connective tissue disorders characterized by excessive bone fragility. Type 3 is a rare form with new mutations; osteopenia and bone fragility are significant with numerous fractures, continuous and severe deformity of the spine, and long bones...

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Detalles Bibliográficos
Autores principales: Augustin, Delange, Augustin, Delange Hendrick, David, Daniel, Théodas, Jefferson Arnold, Derisier, Albertini Fritzlet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925934/
https://www.ncbi.nlm.nih.gov/pubmed/35308738
http://dx.doi.org/10.7759/cureus.22198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925934/
https://www.ncbi.nlm.nih.gov/pubmed/35308738
http://dx.doi.org/10.7759/cureus.22198

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