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Orientador(es)
Resumo(s)
Osteogenesis imperfecta (OI) can cause several ocular manifestations. The most common (and noticeable) is the bluish coloration of the sclerae (+ type I). Other common manifestations include reduced corneal thickness and rigidity, high refractive errors, keratoconus and glaucoma (higher incidence de per se or higher risk?). Less common: scleral rupture, retinal hemorrhages, CNV, among others. The aim of the study: a) assess and explore the ocular features of OI patients in an adult Portuguese population; b) exploratory analysis of relationships between OI types and ocular phenotypes; and c) exploratory analysis of relationships between several variables.
Descrição
Palavras-chave
Rehabilitation Osteogenesis imperfecta Portugal
Contexto Educativo
Citação
Firmino P, Barão R, Pereira D, Sá M, Monteiro P, Silva P, Fonseca AC, Poças I. Ocular changes in OI [osteogenesis imperfecta] in a Portuguese population. In: See, Hear, Smile! Topical Meeting on Osteogenesis Imperfecta, Tallink Hotel, Riga (Latvia), June 14-15, 2019.