TY - CHAP M1 - Book, Section TI - Muckle-Wells Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a very rare genetic disorder with an onset in infancy and characterized by deafness (adolescence), nonpruritic urticaria, and renal amyloidosis type AA. The most common presentation of AA amyloidosis is renal in nature, including proteinuria, nephrotic syndrome and progressive development of renal insufficiency leading to End Stage Renal Disease. Other clinical features include arthralgias and/or conjunctivitis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/04 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164079370 ER -