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Ophthalmological screening guidelines for individuals with Osteogenesis Imperfecta: a scoping review
Autor:
Sarah Moussa, Jasmine Rocci, Reggie Hamdy, Jakob Grauslund, Marie-Louise Lyster, Argerie Tsimicalis
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Osteogenesis imperfecta (OI) is a connective tissue disorder in which the Type 1 collagen is defective. The eye is a structure rich in collagen Type 1 and is heavily impacted by the disease. Many vision-threatening eye diseases ha
Externí odkaz:
https://doaj.org/article/eb79491e127b4c4c97c6f093663c185d
