RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164067702 T1 Delleman Oorthuys Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164067702 RD 2024/03/29 AB It is a rare genetic disorder characterized primarily by eye, skin, and brain malformations that affect almost uniquely males. The clinical features include orbital cysts, focal dermal hypoplasia, vertebral anomalies, craniofacial anomalies, and agenesis of the corpus callosum. Seizure is diagnosed in 50% of patients. The defects are often unilateral with the left side twice more affected than the right. The onset of the disease is at birth.