erythematosus and reveals genetic linkages at 1q22 and 11p13 Thrombocytopenia identifies a severe familial phenotype of systemic lupus

نویسندگان

  • Hal Scofield
  • Gail R Bruner
  • Jennifer A Kelly
  • Jeff Kilpatrick
  • Debra Bacino
  • Swapan K Nath
  • R. Hal Scofield
  • Gail R. Bruner
  • Jennifer A. Kelly
  • Swapan K. Nath
چکیده

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Thrombocytopenia identifies a severe familial phenotype of systemic lupus erythematosus and reveals genetic linkages at 1q22 and 11p13.

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Hematologic manifestation of systemic lupus erythematosus

Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease. The most common hematologic finding is anemia, leukopenia, thrombocytopenia and secondary antiphospholipid syndrome with recurrent abortion and thrombosis. The autoimmune fibrosis of bone marrow is another manifestation of autoimmune disease especially SLE, that must be correctly differentiated from primary myelofibrosis.

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Background: Antiphospholipid antibody syndrome (APS) can either occur as a primary syndrome or associated with other autoimmune diseases such as systemic lupus erythematosus (SLE). Anticardiolipin antibody (aCL) of IgG and/or IgM isotype in blood, measured by a standardized ELISA is the most acceptable laboratory criteria. APS IgG isotype, particularly IgG2 subclass is more strongly associated ...

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تاریخ انتشار 2002