ADAMTS18 and cone-rod dystrophy: In humans, ADAMTS18 mutations are associated with pleomorphic ocular manifestations, including microcornea, ectopic pupils, childhood cataract, night blindness, ectopia lentis, rhegmatogenous retinal detachment, and cone-rod dystrophy (Aldahmesh et al., 2013; Peluso et al., 2013; Chandra et al., 2014).