Membranoproliferative glomerulonephritis type II. Case, diagnosis and comments
- 作者: Tsygin AN1, Kartamysheva NN1, Shklyaev DP1, Leonova LV1, Povilaytite PE1
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- 期: 编号 4 (2011)
- 页面: 60-62
- 栏目: Articles
- URL: https://journals.eco-vector.com/2075-3594/article/view/245987
- ID: 245987
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Membranoproliferative glomerulonephritis type II (dense deposit disease) is a rare glomerular disease with a hallmark sign of presence of electron-dense deposits within the glomerular basement membrane. The disease is caused with uncontrolled activation of alternative complement pathway. Some cases have a genetic origin. Childhood is a predominant age of the onset. The article presents a case report with comments
参考
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- Суханов А.В., Румянцев А.Л., Цыгин А.Н.. Мембранопролиферативный гломерулонефрит 2-го типа (болезнь плотных подоцитов) с быстропрогрессирующим течением. Нефрология и диализ 2003; 5 (4): 399-400.
- Appel B. Gerald, Cook Terence H., Hageman G. et al. Membranoproliferative Glomerulonephritis Type II (Dense Deposit Disease): An Update. J Am Soc Nephrol. 2005; 16: 1392-1404.
- Smith R.J.H., Alexander J., Barlow P.N. Et al. New Approaches to the Treatment of Dense Deposit Disease. J Am Soc Nephrol. 2007; 18: 2447-2456.
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