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GTR Home > Conditions/Phenotypes > Polydactyly-myopia syndrome

Polydactyly-myopia syndrome

Synonyms
Czeizel Brooser syndrome; Postaxial Polydactyly with progressive myopia; Postaxial polydactyly-progressive myopia syndrome
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

An exceedingly rare autosomal dominant developmental anomaly reported in 1986 in nine individuals among four generations of the same family. The syndrome has clinical characteristics of four-limb postaxial polydactyly and progressive myopia. There have been no further descriptions in the literature since 1986. [from SNOMEDCT_US]

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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