Late progressive atrophy in rubella retinopathy

Congenital rubella syndrome is characterised by a triad of sensorineural deafness, congenital cataracts and cardiac defects.Up to 62% of affected patients exhibit bilateral pigmentary retinopathy which is typically regarded as non-progressive in adults [1][2][3][4].We demonstrate a case of progressive rubella retinopathy in a 51-year-old female patient.Fundus autofluorescence imaging shows bilateral extra-foveal atrophic patches (long