RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58081826
T1 Norrie Disease
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=58081826
RD 2024/04/19
AB Rare  inherited  neurodevelopmental  disorder  characterized  by  congenital  bilateral  blindness.  Other  features  can  include  mental  retardation,  mild-to-profound  hearing  loss,  and  cataracts  during  early  infancy.  Phthisis  bulbi  (shrinking  of  the  eye)  has  been  reported.