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

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-year-o...

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Detalhes bibliográficos
Publicado no:BMC Nephrol
Main Authors: Oda, Yasuhiro, Sawa, Naoki, Hasegawa, Eiko, Mizuno, Hiroki, Kawada, Masahiro, Sekine, Akinari, Hiramatsu, Rikako, Yamanouchi, Masayuki, Hayami, Noriko, Suwabe, Tatsuya, Hoshino, Junichi, Takaichi, Kenmei, Kinowaki, Keiichi, Ohashi, Kenichi, Fujii, Takeshi, Ubara, Yoshifumi
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6712641/
https://ncbi.nlm.nih.gov/pubmed/31455242
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-019-1524-6
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