TY - CHAP M1 - Book, Section TI - Laurence Moon Syndrome (LMS) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/04 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164076410 ER -