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Polydactyly-myopia syndrome
rarePolydactyly-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.
- Identifiers
- MONDO:0008268 OMIM:174310Orphanet:2917
- Part of
- Syndromic disease
- Also known as
- Czeizel Brooser syndrome · Czeizel-Brooser syndrome · PMS · polydactyly myopia syndrome · postaxial polydactyly with progressive myopia
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