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dc.contributor.authorAydin, Zeki
dc.contributor.authorKAZANCIOĞLU, Rümeyza
dc.contributor.authorKILIÇASLAN, Işın
dc.contributor.authorOzturk, Savaş
dc.contributor.authorGursu, Meltem
dc.date.accessioned2021-03-08T13:22:39Z
dc.date.available2021-03-08T13:22:39Z
dc.date.issued2010
dc.identifier.citationAydin Z., Gursu M., Ozturk S., KILIÇASLAN I., KAZANCIOĞLU R., "A case of primary immune deficiency presenting with nephrotic syndrome", CLINICAL KIDNEY JOURNAL, cilt.3, sa.5, ss.456-458, 2010
dc.identifier.othervv_1032021
dc.identifier.otherav_36f3517f-15c1-46db-b702-5a58aec3b43f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/167625
dc.identifier.urihttps://doi.org/10.1093/ndtplus/sfq083
dc.description.abstractCommon variable immunodeficiency (CVID) is the most common form of severe antibody deficiency. The disorder is associated with a broad spectrum of clinical manifestations, including infections and chronic lung, gastrointestinal and autoimmune diseases. A 29-year-old female patient has had frequent sinopulmonary infections and gastroenteritis for the last 20 years and had been given broad-spectrum antibiotics for treatment. Immunoglobulin (Ig) levels were at undetectable levels. Renal biopsy was consistent with AA amyloidosis. She is now under follow-up with periodic intravenous Ig treatment without any infection during the last 10 months. CVID must be kept in mind in patients with recurrent sinopulmonary infections.
dc.language.isoeng
dc.subjectNefroloji
dc.subjectNephrology
dc.subjectUrology
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleA case of primary immune deficiency presenting with nephrotic syndrome
dc.typeMakale
dc.relation.journalCLINICAL KIDNEY JOURNAL
dc.contributor.departmentIstanbul Haseki Training & Research Hospital , ,
dc.identifier.volume3
dc.identifier.issue5
dc.identifier.startpage456
dc.identifier.endpage458
dc.contributor.firstauthorID2529108


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