Abstract:【Purpose】We reported a patient with autosomal dominant optic atrophy (ADOA) whose cone contrast threshold had been tested using the ColorDx ® CCT-HD™ (ColorDx). 【Case】The patient was a 38-year-old male. Genetic testing revealed an OPA1 gene mutation and he was diagnosed with ADOA. The best corrected decimal visual acuity was 1.
Set email alert for when this publication receives citations?
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.