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Characterizing inherited retinal diseases involves a detailed medical history, clinical examination with testing of visual function, multimodal retinal imaging as well as molecular genetic testing. This may facilitate a distinction between different inherited retinal diseases, as well as a differentiation from monogenic systemic diseases with retinal involvement, and from mimicking diseases.<\/jats:p>","DOI":"10.1055\/a-1388-7236","type":"journal-article","created":{"date-parts":[[2021,3,30]],"date-time":"2021-03-30T22:38:51Z","timestamp":1617143931000},"page":"249-259","source":"Crossref","is-referenced-by-count":26,"title":["Diagnosis of Inherited Retinal Diseases"],"prefix":"10.1055","volume":"238","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7699-2112","authenticated-orcid":false,"given":"Johannes","family":"Birtel","sequence":"additional","affiliation":[{"name":"Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom"},{"name":"Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom"},{"name":"Department of Ophthalmology, University of Bonn, Bonn, 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