Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic review

PURPOSE: Osteogenesis imperfecta (OI) is a rare inherited heterogeneous connective tissue disorder characterized by bone fragility, low bone mineral density, skeletal deformity and blue sclera. The dominantly inherited forms of OI are predominantly caused by mutations in either the COL1A1 or COL1A2...

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Detalles Bibliográficos
Autores principales: Treurniet, Sanne, Burger, Pia, Ghyczy, Ebba A.E., Verbraak, Frank D., Curro‐ Tafili, Katie R., Micha, Dimitra, Bravenboer, Nathalie, Ralston, Stuart H., de Vries, Ralph, Moll, Annette C., Eekhoff, Elisabeth Marelise W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290710/
https://www.ncbi.nlm.nih.gov/pubmed/34009739
http://dx.doi.org/10.1111/aos.14882

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290710/
https://www.ncbi.nlm.nih.gov/pubmed/34009739
http://dx.doi.org/10.1111/aos.14882

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