1 resultados
Resultados de la búsqueda
Mostrando 1 - 1 de 1
Ítem Mowat-Wilson'S Syndrome: A Case Report(Sociedad Chilena de Pediatría, 2012-08-01) Saldarriaga G, WilmarMowat-Wilson syndrome (MWS) is a very infrequent congenital polimalformative disorder, caused by mutations, deletions or insertions of the ZEB2 gene, which codify for a protein that is involved in the migration of the neural crest cells and the development of middle line structures. The inheritance pattern is autosomal dominant, haplo-insufficient.