RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164076430 T1 Leber Congenital Amaurosis (LCA) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164076430 RD 2024/03/28 AB It is an inherited degenerative disease of the retina that appears at birth or in the first few months of life and is characterized by severely decreased vision manifesting at birth or shortly thereafter. Other ocular anomalies may include sensory (wandering) nystagmus, amaurotic pupils, deep-set eyes, photophobia, and eventually severe vision loss leading to blindness. Central nervous system anomalies have been described in some patients.