Apert Syndrome after Surgery

Apert syndrome is a rare genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis), leading to an abnormal head shape. It also causes fusion of fingers and toes (syndactyly), resulting in webbed or fused digits. In addition to cranial and skeletal abnormalities, individuals with Apert syndrome may experience intellectual disabilities, hearing loss, and vision problems. Here, we present a 3D structure suitable for printing of paediatic patient suffering Apert syndrome who underwent surgery at the clinic.

The model contains one .STL file corresponding to Apert syndrome after the surgery. The model is quite large, it has 252 MB and it can be printed either on the smaller or larger 3D printer. Still, we do recommend to use larger 3D printer.