RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164080428 T1 Oculocerebral with Hypopigmentation Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164080428 RD 2024/10/12 AB Extremely rare inherited disorder that may be apparent at birth (congenital) or during early infancy. It is characterized by hypopigmentation of the skin, silvery-gray hair, and abnormalities of the central nervous system that affect the eyes (microphthalmia) and the oculocerebral functional areas as well as spasticity, mental and physical retardation.