Ectodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia

Article

Abstract: Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congeni

Palabras claves:

adermatoglyphia, Basan syndrome, ectodermal dysplasia, Genodermatosis

Autores:

Campos-Domínguez M., Feito-Rodríguez M., Martínez-González V., Molina-Lopez I., Nieto-Benito L.M., Ricardo Maria Suárez-Fernández

Fuentes:

scopus