TY  - CHAP
M1  - Book, Section
TI  - Muckle-Wells Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Very  rare  genetic  disorder  diagnosed  in  infancy  and  characterized  by  deafness  (adolescence),  nonpruritic  urticaria,  and  renal  amyloidosis  type  AA.  Other  clinical  features  include  arthralgias  and/or  conjunctivitis.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58076696
ER  -