Figure 1.
Figure 1. Estimated fraction of the various forms of ITP based on clinical experience of the authors. (From Cines et al., 2009.1 Used with permission.) SLE, systemic lupus erythematosus; APS, antiphospholipid syndrome; CVID, common variable immune deficiency; CLL, chronic lymphocytic leukemia; APLS, autoimmune lymphoproliferative syndrome; post-tx, post-bone marrow or solid organ transplantation

Estimated fraction of the various forms of ITP based on clinical experience of the authors. (From Cines et al., 2009. Used with permission.) SLE, systemic lupus erythematosus; APS, antiphospholipid syndrome; CVID, common variable immune deficiency; CLL, chronic lymphocytic leukemia; APLS, autoimmune lymphoproliferative syndrome; post-tx, post-bone marrow or solid organ transplantation

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