RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58073852 T1 Leber Congenital Amaurosis (LCA) 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=58073852 RD 2024/03/29 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).