RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164072683 T1 Hereditary Sensory and Autonomic Neuropathy Type II (HSAN II) 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=1164072683 RD 2024/03/29 AB Genetic neurodegenerative disorder characterized by inflammation of the fingers and/or toes with paronychia and whitlows, multiple ulcers (fingers, soles of the feet), and sensory loss in both arms and legs. It affects mostly the transmission of sensory information for pain, temperature, and touch. Type II, congenital sensory neuropathy (also historically known as Morvan’s disease), is characterized by onset of symptoms in early infancy or childhood.