Tecellioglu, Fahriye SecilAkpolat, NusretTabel, YılmazGül, Mehmet2024-08-042024-08-0420212636-7688https://search.trdizin.gov.tr/yayin/detay/482478https://hdl.handle.net/11616/88664Alport 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.eninfo:eu-repo/semantics/openAccessArticle28917911794482478