Review of the literature on Alport syndrome: A rare cause of nephrotic syndrome

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dc.contributor.authorTecellioglu, Fahriye Secil
dc.contributor.authorAkpolat, Nusret
dc.contributor.authorTabel, Yılmaz
dc.contributor.authorGül, Mehmet
dc.date.accessioned2024-08-04T19:42:46Z
dc.date.available2024-08-04T19:42:46Z
dc.date.issued2021
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAlport syndrome is a type IV collagen synthesis disorder characterized by hereditary progressive glomerular disease resulting from glomerular basement membrane injury, often accompanied by hearing loss and ocular defects. The most common form is X-linked Alport syndrome, which accounts for 80% of all cases. Although women mainly present with mild urinary symptoms, end-stage renal disease onsets at an early age in men. An 11-year-old girl was admitted to our hospital with mild bifissure oedema for the last 3 months. This study discusses the clinical, morphological and transmission electron microscopic findings of a rare case of Alport syndrome in the context of the wider literature.en_US
dc.identifier.endpage1794en_US
dc.identifier.issn2636-7688
dc.identifier.issue9en_US
dc.identifier.startpage1791en_US
dc.identifier.trdizinid482478en_US
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/482478
dc.identifier.urihttps://hdl.handle.net/11616/88664
dc.identifier.volume28en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofAnnals of Medical Researchen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleReview of the literature on Alport syndrome: A rare cause of nephrotic syndromeen_US
dc.typeArticleen_US

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