RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164080389
T1 Norrie Disease
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=1164080389
RD 2024/04/19
AB Rare  inherited  neurodevelopmental  disorder  characterized  by  congenital  bilateral  blindness  and  white  pupils.  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.