Kidney transplantation in children and adolescents with C3 glomerulopathy or immune complex membranoproliferative glomerulonephritis: a real-world study within the CERTAIN research network
Complement 3 glomerulopathy (C3G) and immune complex membranoproliferative glomerulonephritis (IC-MPGN) are ultra-rare chronic kidney diseases with an overall poor prognosis, with approximately 40-50% of patients progressing to kidney failure within 10 years of diagnosis. C3G is characterized by a h...
Saved in:
| Main Authors: | , , , , , , , , , , , , , , , , , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
December 2024
|
| In: |
Pediatric nephrology
Year: 2024, Volume: 39, Issue: 12, Pages: 3569-3580 |
| ISSN: | 1432-198X |
| DOI: | 10.1007/s00467-024-06476-5 |
| Online Access: | Verlag, kostenfrei, Volltext: https://doi.org/10.1007/s00467-024-06476-5 |
| Author Notes: | Christian Patry, Nicholas J. A. Webb, Manuel Feißt, Kai Krupka, Jan Becker, Martin Bald, Benedetta Antoniello, Ilmay Bilge, Bora Gulhan, Julien Hogan, Nele Kanzelmeyer, Ozan Ozkaya, Anja Büscher, Anne-Laure Sellier-Leclerc, Mohan Shenoy, Lutz T. Weber, Alexander Fichtner, Britta Höcker, Matthias Meier, Burkhard Tönshoff |
| Summary: | Complement 3 glomerulopathy (C3G) and immune complex membranoproliferative glomerulonephritis (IC-MPGN) are ultra-rare chronic kidney diseases with an overall poor prognosis, with approximately 40-50% of patients progressing to kidney failure within 10 years of diagnosis. C3G is characterized by a high rate of disease recurrence in the transplanted kidney. However, there is a lack of published data on clinical outcomes in the pediatric population following transplantation. |
|---|---|
| Item Description: | Online veröffentlicht: 7. August 2024 Gesehen am 29.09.2025 |
| Physical Description: | Online Resource |
| ISSN: | 1432-198X |
| DOI: | 10.1007/s00467-024-06476-5 |