{Reference Type}: Case Reports
{Title}: Vomer aplasia in a patient carrying a de novo mutation of the TP63 gene (3q27).
{Author}: Schindler A;Guazzarotti L;Mameli C;Urbani E;Mozzanica F;Guerrini L;Zuccotti GV;
{Journal}: Int J Pediatr Otorhinolaryngol
{Volume}: 77
{Issue}: 9
{Year}: Sep 2013
{Factor}: 1.626
{DOI}: 10.1016/j.ijporl.2013.06.027
{Abstract}: 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.