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- W2398632956 abstract "Severe combined immunodeficiencies (SCIDs) are a heterogeneous group of diseases characterized by profound compromise of both T lymphocyte and B lymphocyte numbers and/or function. From a descriptive standpoint, SCID can be categorized based on the composition of the peripheral blood lymphocyte populations observed in affected patients. While many forms of SCID present with both T cell and B cell lymphopenia (T − B − SCID), in one group of such disorders B cell differentiation is conserved and normal or even elevated numbers of peripheral blood B lymphocytes can be observed. These diseases are called SCID T − B + and include the X-linked form of SCID (SCIDX-1), the deficiency of Janus kinase family member 3 (JAK3-SCID), and the defect of expression of the alpha chain of the interleukin-7 receptor (IL7-Rα-SCID). This article describes the main features of these rare clinical entities." @default.
- W2398632956 created "2016-06-24" @default.
- W2398632956 creator A5062385004 @default.
- W2398632956 date "2016-01-01" @default.
- W2398632956 modified "2023-09-24" @default.
- W2398632956 title "Combined T Cell and B Cell Deficiency – SCID Forms: T − B +" @default.
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- W2398632956 doi "https://doi.org/10.1016/b978-0-12-374279-7.18003-8" @default.
- W2398632956 hasPublicationYear "2016" @default.
- W2398632956 type Work @default.