RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164076410 T1 Laurence Moon Syndrome (LMS) 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=1164076410 RD 2024/10/03 AB This is a genetic disorder characterized by retinitis pigmentosa (pigmentary degeneration of retina and rod cone dystrophy), ophthalmoplegia, spastic paraplegia, mental retardation, and cardiomyopathy. Other features include obesity, deafness, cataract, polydactyly, and renal insufficiency.