Orbitomalar/zygomatic arch hypoplasia is present in all patients with Treacher Collins Syndrome.
Defects include:
The incomplete or absent zygomatic arch along with an open lower orbital rim will give rise to a downward slanting of the eye.
Coloboma is highly specific for Treacher Collins Syndrome, however it is not present in every case.
Lacrimal system anomalies are also common, this includes atresia of the lacrimal puncta and canaliculi.