RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164066018 T1 Cockayne Syndrome 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=1164066018 RD 2024/10/07 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.