Myeloperoxidase-antineutrophil cytoplasmic antibody-associated crescentic glomerulonephritis in autosomal dominant polycystic kidney disease

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder that is characterized by the development of cysts in the kidneys and other organs. Urinary protein excretion is usually less than 1 g/day, and ADPKD is rarely associated with nephrotic syndrome or rapidly progr...

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Bibliografske podrobnosti
Main Authors: Sumida, Keiichi, Ubara, Yoshifumi, Hoshino, Junichi, Hayami, Noriko, Suwabe, Tatsuya, Hiramatsu, Rikako, Hasegawa, Eiko, Yamanouchi, Masayuki, Sawa, Naoki, Takaichi, Kenmei, Ohashi, Kenichi
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2013
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3644260/
https://ncbi.nlm.nih.gov/pubmed/23617397
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2369-14-94
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