Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome

Background Pathological findings in Alport syndrome frequently show mesangial proliferation and sometimes incidental IgA deposition, in addition to unique glomerular basement membrane (GBM) changes including thin basement membrane and/or lamellation. However, similar GBM abnormalities are also often...

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Veröffentlicht in:	Clinical and experimental nephrology 2021-07, Vol.25 (7), p.779-787
Hauptverfasser:	Ishiko, Shinya, Tanaka, Akihito, Takeda, Asami, Hara, Masayuki, Hamano, Naoto, Koizumi, Masahiro, Ueno, Toshinori, Hayashi, Hiroki, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Sakakibara, Nana, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Ninchoji, Takeshi, Shima, Yuko, Nakanishi, Koichi, Yoshikawa, Norishige, Iijima, Kazumoto, Nozu, Kandai
Format:	Artikel
Sprache:	eng
Schlagworte:	Alport syndrome Collagen (type IV) Differential diagnosis Galactose Hematuria IgA nephropathy Immunoglobulin A Medicine Medicine & Public Health Monoclonal antibodies Nephrology Original Article Proteinuria Toxicity Urology
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