Polydactyly-myopia syndrome is an exceedingly rare autosomal dominant developmental anomaly reported in 1986 in nine individuals among four generations of the same family. The syndrome is characterized clinically by four-limb postaxial polydactyly and progressive myopia. There have been no further descriptions in the literature since 1986. The disease is MONDO_0008268 (polydactyly-myopia syndrome). Also known as: Czeizel-Brooser syndrome.