QR-kod

PKD1-associated autosomal dominant polycystic kidney disease with glomerular cysts presenting with nephrotic syndrome caused by focal segmental glomerulosclerosis

Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) may manifest non-nephrotic range proteinuria, but is rarely complicated with nephrotic syndrome. Limited number of reports describe the histology of ADPKD with nephrotic syndrome in detail. Case presentation We encountered a 23...

Full beskrivning

Sparad:
Huvudupphov: Yasuhiro Oda, Naoki Sawa, Eiko Hasegawa, Hiroki Mizuno, Masahiro Kawada, Akinari Sekine, Rikako Hiramatsu, Masayuki Yamanouchi, Noriko Hayami, Tatsuya Suwabe, Junichi Hoshino, Kenmei Takaichi, Keiichi Kinowaki, Kenichi Ohashi, Takeshi Fujii, Yoshifumi Ubara
Materialtyp: Artigo
Språk:Inglês
Utgiven: BMC 2019-08-01
Serie:BMC Nephrology
Ämnen:
Autosomal dominant polycystic kidney disease
PKD1
Glomerular cyst
Focal segmental glomerulosclerosis
Länkar:http://link.springer.com/article/10.1186/s12882-019-1524-6
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk