TY - CHAP M1 - Book, Section TI - Delleman Oorthuys Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164067702 ER -