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Rheumatology Advance Access originally published online on October 14, 2009
Rheumatology 2009 48(12):1618-1619; doi:10.1093/rheumatology/kep321
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© The Author 2009. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Brain multiple sclerosis-like lesions in a patient with Muckle–Wells syndrome

Sandrine Compeyrot-Lacassagne1, Tu-Anh Tran1,2, Séverine Guillaume-Czitrom1, Isabelle Marie1,2 and Isabelle Koné-Paut1,2

1Division of Pediatric Rheumatology and 2Division of Pediatrics, Bicêtre University Hospital, Le Kremlin Bicêtre Cedex, France

Correspondence to: Sandrine Compeyrot-Lacassagne, Division of Pediatric Rheumatology, Bicêtre University Hospital, 78, Rue du Général Leclerc, 94275 Le Kremlin Bicêtre Cedex, France. E-mail: sandrine.lacassagne@bct.aphp.fr

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SIR, Muckle–Wells syndrome (MWS) is an autosomal dominant condition with variable penetrance characterized by recurrent fever syndromes, urticarial rash, non-exudative conjunctivitis, myalgia, arthralgia and/or arthritis, chronic headaches and/or increased intracranial pressure, chronic deafness and decreased level of energy [1]. MWS belongs to the group of cryopyrin-associated periodic fever (CAPS) including familial cold . . . [Full Text of this Article]


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