syndromic disease polydactyly-myopia syndrome https://rarediseases.info.nih.gov/diseases/4413/polydactyly-myopia-syndrome https://www.malacards.org/card/polydactyly_postaxial_with_progressive_myopia postaxial polydactyly with progressive myopia postaxial polydactyly-progressive myopia syndrome SCTID:82639001 GARD:0004413 polydactyly-myopia syndrome MESH:C536331 OMIM:174310 PMS MEDGEN:357424 polydactyly myopia syndrome MONDO:0008268 Orphanet:2917 Czeizel Brooser syndrome Czeizel-Brooser syndrome 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. ICD9:625.4 UMLS:C1868117