ba0006p119 | (1) | ICCBH2017
Rubino Chiara
, Stagi Stefano
, Petrolini Chiara
, Gioe Daniela
, La Spina Luisa
, Peluso Francesca
, Della Monica Matteo
, de Martino Maurizio
Background: Weyers acrofacial dysostosis (WAD, OMIM 193530) is a rare autosomal dominant disease, characterized by mildly short stature, postaxial polydactyly, nail dystrophy and dental anomalies. WAD should be distinguished from Ellis-van Creveld syndrome (OMIM 225500), a similar but more severe disease, comprising chondrodysplasia, orofacial anomalies and, in a proportion of patients, cardiovascular malformations. Both diseases are caused by mutations in either EVC or EVC2<s...