S 錐体系のコントラスト感度低下を認めた常染色体顕性（優性）視神経萎縮の1例

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.