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Abstract
Glomerular thrombotic microangiopathy is a hallmark feature of haemolytic uraemic syndrome, the leading cause of acute renal failure in childhood. This paper is a review of the different mechanistic pathways that lead to this histological picture in the kidney. It will focus on atypical HUS and complement dysregulation, but will also highlight some other recent advances in our understanding of this condition, including the potential role of the molecule vascular endothelial growth factor- A (VEGF-A).
| Original language | English |
|---|---|
| Pages (from-to) | 523-533 |
| Number of pages | 11 |
| Journal | Pediatric Nephrology |
| Volume | 26 |
| Issue number | 4 |
| Early online date | 15 Oct 2010 |
| DOIs | |
| Publication status | Published - 1 Apr 2011 |
Bibliographical note
Publisher Copyright:© IPNA 2010
Keywords
- Humans
- Kidney Glomerulus/metabolism
- Purpura, Thrombotic Thrombocytopenic/metabolism
- Thrombotic Microangiopathies/metabolism
- Vascular Endothelial Growth Factor A/metabolism
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