Publication:
Hereditary Spherocytosis With Immunoglobulin A Nephropathy

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dc.contributor.authorsBiyikli, Nese Karaaslan; Gokce, Ibrahim; Cakalagaoglu, Fulya; Turkkan, Emine; Alpay, Harika
dc.date.accessioned2022-03-12T17:48:32Z
dc.date.accessioned2026-01-10T17:26:57Z
dc.date.available2022-03-12T17:48:32Z
dc.date.issued2010
dc.description.abstractHereditary spherocytosis is a familial hemolytic anemia. Immunoglobulin A (IgA) nephropathy associated with hereditary spherocytosis has not been reported in children. Here, we report a case of a 17-year-old boy with IgA nephropathy and hereditary spherocytosis. The patient was diagnosed with hereditary spherocytosis at the age of 12 years and splenectomy was done at the age of 15 years. Later, the patient presented with macroscopic hematuria and proteinuria. Kidney biopsy of the boy was consistent with IgA nephropathy. Treatment with angiotensin-converting enzyme inhibitor was started. The patient became free of proteinuria after the 6th month of therapy. IJKD 2010;4:78-81 www.ijkd.org
dc.identifier.doidoiWOS:000297078000014
dc.identifier.eissn1735-8604
dc.identifier.issn1735-8582
dc.identifier.pubmed20081310
dc.identifier.urihttps://hdl.handle.net/11424/229971
dc.identifier.wosWOS:000297078000014
dc.language.isoeng
dc.publisherIRANIAN SOC NEPHROLGY
dc.relation.ispartofIRANIAN JOURNAL OF KIDNEY DISEASES
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectIgA glomerulonephritis
dc.subjecthereditary spherocytosis
dc.subjectchild
dc.subjecthemolytic anemia
dc.subjectHEMOLYTIC-ANEMIA
dc.subjectGLOMERULONEPHRITIS
dc.subjectNEPHRITIS
dc.titleHereditary Spherocytosis With Immunoglobulin A Nephropathy
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage81
oaire.citation.issue1
oaire.citation.startPage78
oaire.citation.titleIRANIAN JOURNAL OF KIDNEY DISEASES
oaire.citation.volume4

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