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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Design, development and deployment of a web-based interoperable registry for inherited retinal dystrophies in Portugal: the IRD-PT

Fig. 1

Variation in the percentage of eyes with different levels of BCVA (ETDRS letters) over time (last-observation carried forward) in the 45 patients (90 eyes) with Usher syndrome included in the IRD-PT registry so far. The graph is automatically provided by the platform. The user may select which parameters to show. It is also possible to select only one eye per patient

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172