TY  - CHAP
M1  - Book, Section
TI  - Leber Congenital Amaurosis (LCA)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Inherited  degenerative  disease  of  the  retina  characterized  by  severely  decreased  vision  manifesting  at  birth  or  shortly  thereafter.  Other  ocular  anomalies  may  include  sensory  (wandering)  nystagmus,  amaurotic  pupils,  deep-set  eyes,  and  photophobia.  Central  nervous  system  anomalies  have  been  described  in  some  patients.  Do  not  confuse  with  Leber  hereditary  optic  neuropathy  (see  Leber  Hereditary  Optic  Neuropathy).  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58073852
ER  -