Weyers acrofacial dysostosis

info · Genetic

An acrofacial dysostosis characterized by dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature that has_material_basis_in heterozygous mutation in the genes EVC2 or EVC on chromosome 4p16.2.

Signs and symptoms

Prominent antihelix
Small nail
Short palm
Brachydactyly
Postaxial hand polydactyly
Nail dysplasia
Hypotelorism
Clinodactyly of the 5th finger
Postaxial foot polydactyly
Solitary median maxillary central incisor

Also known as: Curry-Hall syndrome; WAD; Weyers acrodental dysostosis; acrofacial dysostosis, Weyers type