An unusual complication after craniofacial surgery for Apert syndrome
Apert syndrome is a rare genetic disorder, characterized by premature fusion of skull sutures, mid-face hypoplasia and syndactyly of the hands and feet.It is inherited as autosomal dominant or sporadic and is associated with increased paternal age.It arises from mutations in the fibroblast growth factor receptor shure blx2 h10 2 gene on chromosome