Familial Muller cell sheen dystrophy associated with congenital color vision deficiency

A coincidence of Muller cell sheen dystrophy (MCSD) and congenital color vision deficiency in a 36 years old man is presented in this case report. Best corrected visual acuity (BCVA) was 1.0 in both eyes. He failed to read Ishihara color plates (0/13 in both eyes). Dilated fundus examination showed bilateral wrinkled glistening inner retinal surface at the posterior pole. In the macular images of optical coherence tomography, internal limiting membrane layer had an undulating view. Maternal ocular examination and color vision test revealed no pathology. His father was not alive, and he had no pedigree. To our knowledge this is the first case in the literature, diagnosed with MCSD associated with congenital color vision deficiency.