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A patient with Wells’ syndrome

✍ Scribed by E. Ladoyanni; C. Vlachou; R. Thushara; D. Snead

Book ID
108695052
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
794 KB
Volume
35
Category
Article
ISSN
0307-6938

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## Abstract Muckle‐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 interleukin‐1β (IL‐1β). In this report we describe an 8‐year‐old