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MPGN II - genetically determined by defective complement regulation?

MPGN II is a rare disease which is characterized by complement containing deposits within the GBM. The disease is characterized by functional impairment of the GBM causing progressive loss of renal function eventually resulting in end stage renal disease.

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Bibliographic Details
Main Authors: Licht, Christoph (Author) , Schlötzer-Schrehardt, Ursula (Author) , Kirschfink, Michael (Author) , Zipfel, Peter F. (Author) , Hoppe, Bernd (Author)
Format: Article (Journal)
Language:English
Published: 2007
In: Pediatric nephrology
Year: 2007, Volume: 22, Issue: 1, Pages: 2-9
ISSN:1432-198X
DOI:10.1007/s00467-006-0299-8
Online Access:Verlag, lizenzpflichtig, Volltext: https://dx.doi.org/10.1007/s00467-006-0299-8
Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00467-006-0299-8
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Author Notes:Christoph Licht, Ursula Schlötzer-Schrehardt, Michael Kirschfink, Peter F. Zipfel, Bernd Hoppe
Description
Summary:MPGN II is a rare disease which is characterized by complement containing deposits within the GBM. The disease is characterized by functional impairment of the GBM causing progressive loss of renal function eventually resulting in end stage renal disease.
Item Description:published online: 23 September 2006
Gesehen am 15.02.2021
Physical Description:Online Resource
ISSN:1432-198X
DOI:10.1007/s00467-006-0299-8

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