RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58081915
T1 Oculocerebral with Hypopigmentation Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58081915
RD 2024/09/19
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.