Choroidopathy was found to be the dominant ocular feature in KIF11-related retinopathy in cases with MCLMR, which is commonly described as focal choroidal atrophy or dysplasia with variable phenotypes ranging from mild RPE damage to diffuse choroidal dysplasia [10]. Here, KIF11 is linked to microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability.