RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164083121 T1 Rabson-Mendenhall 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=1164083121 RD 2024/03/29 AB An extremely rare genetic disorder characterized by severe insulin resistance and craniofacial anomalies, abnormalities of the teeth and nails, and acanthosis nigricans (hyperpigmentation and hyperkeratosis), particularly of the neck, groin, and underarms.