%0 Case Reports
%T Vomer aplasia in a patient carrying a de novo mutation of the TP63 gene (3q27).
%A Schindler A
%A Guazzarotti L
%A Mameli C
%A Urbani E
%A Mozzanica F
%A Guerrini L
%A Zuccotti GV
%J Int J Pediatr Otorhinolaryngol
%V 77
%N 9
%D Sep 2013
%M 23906991
%F 1.626
%R 10.1016/j.ijporl.2013.06.027
%X The congenital vomer defect (CVD) is a rare and still partially unknown condition. Only few cases have been reported in the international literature and the large majority of them appeared to be isolated. We report a case of CVD detected in a 7-year-old girl affected by ectodermal dysplasia clefting syndrome caused by a mutation of the TP63 gene.