Macular neovascularisation in a patient with osteogenesis imperfecta exhibiting a novel COL1A1 mutation

Osteogenesis imperfecta is a congenital disease that presents with varying degrees of connective tissue symptoms, including susceptibility to fracture, growth disorders and hearing loss. Here, we discuss a case in which macular neovascularisation (MNV) resulted in metamorphopsia and decreased visual...

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Detalles Bibliográficos
Autores principales: Sato, Yoshiki, Kimoto, Kenichi, Takaki, Yasuhiro, Kubota, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Case Reports: Rare disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644304/
https://www.ncbi.nlm.nih.gov/pubmed/36343986
http://dx.doi.org/10.1136/bcr-2022-251763

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644304/
https://www.ncbi.nlm.nih.gov/pubmed/36343986
http://dx.doi.org/10.1136/bcr-2022-251763

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