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Recovery from deafness in a patient with Muckle-Wells syndrome treated with anakinra

โœ Scribed by Tristan Mirault; David Launay; Laurence Cuisset; Eric Hachulla; Marc Lambert; Viviane Queyrel; Thomas Quemeneur; Sandrine Morell-Dubois; Pierre-Yves Hatron


Book ID
101647729
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
57 KB
Volume
54
Category
Article
ISSN
0004-3591

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## Abstract Muckleโ€Wells syndrome (MWS) is a dominantly inherited autoinflammatory syndrome. Patients with MWS have a mutation in __CIAS1__, the gene encoding cryopyrin, a component of the inflammasome that regulates the processing of interleukinโ€1ฮฒ (ILโ€1ฮฒ). In this report we describe an 8โ€yearโ€old