KIF11 and microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability: Mutations in KIF11 have been known to be a cause of an autosomal dominant inherited disease characterized by microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR: OMIM#152950, ORPHA#2526) [2,3].