TY - CHAP M1 - Book, Section TI - Rabson-Mendenhall Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164083121 ER -