Review of the literature on Alport syndrome: A rare cause of nephrotic syndrome
| dc.contributor.author | Tecellioglu, Mehmet | |
| dc.contributor.author | Akpolat, Nusret | |
| dc.contributor.author | Tabel, Yilmaz | |
| dc.contributor.author | Gul, Mehmet | |
| dc.date.accessioned | 2022-03-15T15:39:48Z | |
| dc.date.available | 2022-03-15T15:39:48Z | |
| dc.date.issued | 2021 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Alport 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.citation | Tecellioglu, F. S., Akpolat, N., Tabel, Y., & Gul, M. (2021). Review of the literature on Alport syndrome: A rare cause of nephrotic syndrome. Annals of Medical Research, | en_US |
| dc.identifier.uri | https://hdl.handle.net/11616/55747 | |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Annals of Medical Research | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Review of the literature on Alport syndrome: A rare cause of nephrotic syndrome | en_US |
| dc.type | Article | en_US |
