| Literature DB >> 22678748 |
Bertrand Isidor1, Sylvaine Poignant, Georges Picherot, André Mégabarné, Pierre Quartier, Brigitte Bader-Meunier, Cédric Le Caignec, Martine Le Merrer, Geneviève Baujat, Valérie Cormier-Daire, Albert David.
Abstract
Juvenile idiopathic arthritis is an inflammatory disease with various onset-forms which can sometimes be difficult to distinguish from genetic inflammatory/rheumatoid-like osteoarthropathies. In this report, we describe two boys with severe chronic arthralgia, stiffness and swelling of joints, motor weakness and joints contractures evolving despite immunosuppressive treatments and for whom all biological and molecular exams failed to identify a prompt diagnosis. Some findings also overlap with pseudorheumatoid dysplasia but WISP3 gene molecular analysis failed to identify any mutation for both patients. Therefore, we propose that these boys show a clinical entity distinct from the actually known genetic inflammatory/rheumatoid-like osteoarthropathies.Entities:
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Year: 2012 PMID: 22678748 DOI: 10.1002/ajmg.a.35424
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802