TY - CHAP M1 - Book, Section TI - Oculocerebral with Hypopigmentation Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/11 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164080428 ER -