RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164061334 T1 Allgrove Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164061334 RD 2024/03/29 AB A genetic disease characterized by the triad of adrenocorticotropic hormone (ACTH)-resistant adrenal insufficiency, achalasia, and alacrima. It presents in the first decade of life with severe and potentially fatal hypoglycemic episodes. A mixed pattern of upper and lower motor neuropathy, sensory impairment, autonomic neuropathy, and mental retardation is common.