TY - CHAP M1 - Book, Section TI - Leber Congenital Amaurosis (LCA) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164076430 ER -