TY - CHAP M1 - Book, Section TI - Cockayne Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A complex inherited disorder characterized by the association of dwarfism, deafness, microcephaly, facial anomalies, ataxia, photosensitivity, retinal atrophy, and renal insufficiency with premature aging and atherosclerosis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/08 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164066018 ER -