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Corneal tomography in osteogenesis imperfecta

dc.contributor.authorBarão, R.
dc.contributor.authorMarques, R. E.
dc.contributor.authorMano, S. S.
dc.contributor.authorFirmino, Patrícia
dc.contributor.authorPoças, Ilda Maria
dc.contributor.authorRodrigues, W.
dc.contributor.authorFonseca, A. C.
dc.contributor.authorGuerra, P.
dc.date.accessioned2021-08-03T10:35:08Z
dc.date.available2021-08-03T10:35:08Z
dc.date.issued2020-06
dc.description.abstractOsteogenesis Imperfecta (OI) is a rare genetic disorder with musculoskeletal manifestations and some ocular features, such as the presence of blue sclerae, corneal thinning, altered corneal biomechanics, and rare reports of keratoconus (KC). Corneal tomography is essential for KC screening and a BAD_D score over 1,6 and 2,6 is highly sensitive and specific for the detection of subclinical KC and keratoconic corneas, respectively. This study aims to explore the corneal tomographic characteristics of OI patients.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBarão R, Marques RE, Mano SS, Firmino P, Poças I, Rodrigues W, et al. Corneal tomography in osteogenesis imperfecta. In: WOC 2020 – World Ophthalmology Congress [online], June 26-29, 2020.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.21/13608
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relation.publisherversionhttps://icowoc.org/pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectOrthopticspt_PT
dc.subjectOsteogenesis imperfectapt_PT
dc.subjectCorneal tomographypt_PT
dc.titleCorneal tomography in osteogenesis imperfectapt_PT
dc.typeconference object
dspace.entity.typePublication
person.familyNamePoças
person.givenNameIlda Maria
person.identifier.ciencia-id1E1A-86A4-BC50
person.identifier.orcid0000-0002-1695-3231
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublicationced35a9f-848a-49c9-91dc-f60f679f149f
relation.isAuthorOfPublication.latestForDiscoveryced35a9f-848a-49c9-91dc-f60f679f149f

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