Publication: Other well-defined immunodeficiency syndromes
| dc.contributor.authors | Espanol T., Fillat C., Barlan I.B., Aydiner E., Caracseghi F., Niehues T., Soler-Palacín P., Rezaei N. | |
| dc.date.accessioned | 2022-03-15T02:09:37Z | |
| dc.date.accessioned | 2026-01-10T18:41:28Z | |
| dc.date.available | 2022-03-15T02:09:37Z | |
| dc.date.issued | 2012 | |
| dc.description.abstract | Five broad and major groups of PID classification have been known as CID, PAD, phagocyte disorders, complement deficiencies, as well as other well-defined immunodeficiency syndromes. The former includes Wiskott-Aldrich syndrome (WAS), which presents as a clinical triad of eczema, thrombocytopenia, and recurrent infections. Patients exhibit a variety of laboratory abnormalities, including decreases in peripheral blood CD8+ T cells. A flow cytometric assay for the detection of Wiskott-Aldrich syndrome protein (WASP) protein in lymphocytes has recently been described and applied to the diagnostic evaluation of both WAS patients and carriers of WASP mutations [1]. © Springer-Verlag Berlin Heidelberg 2012. | |
| dc.identifier.doi | 10.1007/978-3-642-31785-9_9 | |
| dc.identifier.isbn | 9783642317859; 9783642317842 | |
| dc.identifier.uri | https://hdl.handle.net/11424/247220 | |
| dc.language.iso | eng | |
| dc.publisher | Springer Berlin Heidelberg | |
| dc.relation.ispartof | Clinical Cases in Primary Immunodeficiency Diseases: A Problem-Solving Approach | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.title | Other well-defined immunodeficiency syndromes | |
| dc.type | bookPart | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 368 | |
| oaire.citation.startPage | 343 | |
| oaire.citation.title | Clinical Cases in Primary Immunodeficiency Diseases: A Problem-Solving Approach |