Renal Amyloidosis in a Common Variable Immune Deficiency Patient with Autoimmune Complications

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dc.contributor.authorArslan, Şevket
dc.contributor.authorYıldız, Eray
dc.contributor.authorEsen, Hacı Hasan
dc.contributor.authorAytekin, Gökhan
dc.contributor.authorÇölkesen, Fatih
dc.date.accessioned2023-04-10T20:19:30Z
dc.date.available2023-04-10T20:19:30Z
dc.date.issued2020
dc.departmentRektörlük, Rektörlüğe Bağlı Birimler, Düzce Üniversitesi Dergilerien_US
dc.description.abstractCommon variable immune deficiency (CVID) is a rare primary immunodeficiency disorderthat is characterized by defective antibody production and inadequate B cell differentiation.While frequently recurrent respiratory tract infections are the most prominent clinical featurein CVID patients, CVID is a heterogeneous immune deficiency disorder that involves manysystems and organs such as lymphoid hyperplasia, autoimmune cytopenia, chronic lungdiseases, granulomatous diseases and susceptibility to malignancy. This may lead to delay indiagnosis and immunoglobulin replacement therapy, not being able to receive antibiotics at theappropriate dose and time, chronic inflammation, and therefore secondary amyloidosis. In thiscase report it is aimed to present a CVID patient with autoimmune complications anddeveloping renal amyloidosis during follow-up.en_US
dc.identifier.doi10.18678/dtfd.693297
dc.identifier.endpage70en_US
dc.identifier.issn1307-671X
dc.identifier.issue1en_US
dc.identifier.startpage67en_US
dc.identifier.trdizinid385777en_US
dc.identifier.urihttp://doi.org/10.18678/dtfd.693297
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/385777
dc.identifier.urihttps://hdl.handle.net/20.500.12684/11386
dc.identifier.volume22en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofDüzce Tıp Fakültesi Dergisi
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleRenal Amyloidosis in a Common Variable Immune Deficiency Patient with Autoimmune Complicationsen_US
dc.typeArticleen_US

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