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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712641/
https://www.ncbi.nlm.nih.gov/pubmed/31455242
http://dx.doi.org/10.1186/s12882-019-1524-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712641/
https://www.ncbi.nlm.nih.gov/pubmed/31455242
http://dx.doi.org/10.1186/s12882-019-1524-6

Ejemplares similares