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Schnitzler Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • An extremely rare condition manifested as monoclonal IMMUNOGLOBULIN M dysproteinemia without features of lymphoproliferative disease, but with chronic urticaria, fever of unknown origin, disabling bone pain, hyperostosis, and increased erythrocyte sedimentation rate.

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-MRQ78NR1-8

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