QJM, Vol 91, Issue 7 489-492, Copyright © 1998 by Oxford University Press
AW Gerbig, CA Dahinden, P Mullis and T Hunziker
Muckle-Wells syndrome (MWS) is a rare autosomal dominant hereditary
disorder characterized by chronic recurrent urticaria, arthralgia,
sensorineural deafness, and in some cases nephropathy due to amyloidosis
(AA type). We report a 21-year-old woman and her father, both suffering
from this syndrome, in whom elevated serum levels of IL- 6 could be
documented during the flares of urticaria, and discuss the relevance of
this finding for MWS.
ORIGINAL PAPERS
Circadian elevation of IL-6 levels in Muckle-Wells syndrome: a disorder of the neuro-immune axis?
Department of Dermatology, University of Bern, Switzerland.
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