TY - CHAP M1 - Book, Section TI - Oculocerebral with Hypopigmentation Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. Y1 - 2006 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications 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. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58081915 ER -