Patient with fundus albipunctatus associated with cone dystrophy. Fundi with numerous white punctata scattered over the retinal pigment epithelium of both eyes as well as macular atrophic lesions. The patient shows relative central scotomas on static perimetry,reduced foveal thickness on OCT and reduced amplitude with recovery to normal values after 3 hours of dark adaption on the scotopic ff ERG. The ff cone and 30-Hz flicker ERGs were also significantly reduced thus suggesting the association of fundus albipunctatus with cone dystrophy.