RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164079370
T1 Muckle-Wells 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=1164079370
RD 2024/04/24
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.