RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164083867 T1 Rombo 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=1164083867 RD 2024/03/29 AB Genetic disorder characterized by facial follicular skin atrophy, milia, telangiectasias, absent eyelashes and eyebrows, and basal cell carcinomas later on in life.