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.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 |
http://hdl.handle.net/11616/55747 |
|
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.language.iso |
eng |
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 |
dc.relation.journal |
Annals of Medical Research |
en_US |
dc.contributor.department |
İnönü Üniversitesi |
en_US |