TY - CHAP M1 - Book, Section TI - Rombo Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Genetic disorder characterized by facial follicular skin atrophy, milia, telangiectasias, absent eyelashes and eyebrows, and basal cell carcinomas later on in life. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164083867 ER -