The patient clinical journey and socioeconomic impact of osteogenesis imperfecta: a systematic scoping review

BACKGROUND: Osteogenesis imperfecta (OI) is a rare heritable connective tissue disorder primarily characterised by skeletal deformity and fragility, and an array of secondary features. The purpose of this review was to capture and quantify the published evidence relating specifically to the clinical...

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Detalles Bibliográficos
Autores principales: Rapoport, Maria, Bober, Michael B., Raggio, Cathleen, Wekre, Lena Lande, Rauch, Frank, Westerheim, Ingunn, Hart, Tracy, van Welzenis, Taco, Mistry, Arun, Clancy, James, Booth, Lucy, Prince, Samantha, Semler, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945474/
https://www.ncbi.nlm.nih.gov/pubmed/36814274
http://dx.doi.org/10.1186/s13023-023-02627-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945474/
https://www.ncbi.nlm.nih.gov/pubmed/36814274
http://dx.doi.org/10.1186/s13023-023-02627-3

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