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Collagenofibrotic glomerulopathy – rare glomerulonephritis


Authors: G. Bernasovská 1;  M. Demeš 1;  A. Okša 1,2;  M. Pavlovič 1;  A. Vahančík 1;  O. Nyitrayová 3;  P. Gomolčák 3;  D. Daniš 3
Authors‘ workplace: I. interná klinika Slovenskej zdravotníckej univerzity a FNsP Bratislava, pracovisko Kramáre, Slovenská republika, prednosta prim. prof. MUDr. Štefan Hrušovský, CSc., Dr. SVS 1;  Oddelenie klinickej a experimentálnej farmakoterapie Slovenskej zdravotníckej univerzity Bratislava, Slovenská republika, vedúci h. doc. MUDr. Martin Gajdoš, CSc. 2;  Ústav patológie FNsP Bratislava, pracovisko Kramáre, Slovenská republika, vedúci doc. MUDr. Dušan Daniš, CSc 3
Published in: Vnitř Lék 2006; 52(12): 1200-1204
Category: Case Report

Práca bola prednesená 19. 9. 2004 na sympóziu s medzinárodnou účasťou Kvalita starostlivosti o nefrologického, dialyzovaného a transplantovaného pacienta, Zemplínska Šírava, Slovenská republika.

Overview

Glomerulopathies with fibrillary deposits form a heterogeneous group of renal diseases that can be identified only by means of electron microscopy. A case of rare type of such a nephropathy, the collagenofibrotic glomerulopathy with focus on differential diagnostics is presented and a review of current knowledge on this renal disease is given.

Key words:
fibrillary glomerulopathies - collagenofibrotic glomerulopathy - electron microscopy


Sources

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Labels
Diabetology Endocrinology Internal medicine

Article was published in

Internal Medicine

Issue 12

2006 Issue 12

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