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dc.contributor.authorKutlu, Orkide
dc.contributor.authorTukek, Tufan
dc.contributor.authorEruzun, Hasan
dc.date.accessioned2021-03-06T08:33:00Z
dc.date.available2021-03-06T08:33:00Z
dc.date.issued2016
dc.identifier.citationKutlu O., Eruzun H., Tukek T., "COMMON VARIABLE IMMUNODEFICIENCY", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.79, ss.122-129, 2016
dc.identifier.othervv_1032021
dc.identifier.otherav_e17f5a3a-4985-409a-8ddc-b0be2d7c2ae2
dc.identifier.urihttp://hdl.handle.net/20.500.12627/148449
dc.identifier.urihttps://doi.org/10.1111/cei.12884
dc.description.abstractCommon variable immunodeficiency is the most commonly seen primary immune deficiency condition in adults, characterized by impaired B cell differentiation. The patient is diagnosed with common variable immunodeficiency by recurrent bacterial infections usually accompanied by chronic lung diseases, gastrointestinal/liver diseases, granulomatous diseases, autoimmunity, lymphoid hyperplasia, splenomegaly or malignancies. Serum IgG concentration is significantly low along with low IgA and/or IgM concentrations. Intravenous immunoglobulin (IVIG) is the first choice of treatment. Immunoglobulin treatment ameliorates recurrent infections and associated complications such as autoimmune diseases and pulmonary injury. The main cause of death in patients with common variable immunodeficiency is chronic lung diseases or malignancies, because acute bacterial infections is usually prevented by IVIG therapy.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleCOMMON VARIABLE IMMUNODEFICIENCY
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.departmentIstanbul Okmeydani Training & Research Hospital , ,
dc.identifier.volume79
dc.identifier.issue3
dc.identifier.startpage122
dc.identifier.endpage129
dc.contributor.firstauthorID227881


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