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A rare glomerular disease characterized by abnormal accumulation of type III collagen within the mesangium and subendothelial space of the glomerulus. Clinically it usually manifests with proteinuria (often in the nephrotic range), microscopic hematuria, peripheral edema and/or hypertension. In some cases progression to end-stage renal failure is observed.
No clinical trials have been registered for collagen type III glomerulopathy.
8 publications have been identified in PubMed for collagen type III glomerulopathy. Research spans Case Report / Case Series (88%) and Review / Meta-Analysis (13%).
Večerić-Haler Ž (2026). [PMID: 41776468](https://pubmed.ncbi.nlm.nih.gov/41776468/). *BMC nephrology*. [Review / Meta-Analysis]
Yamamoto S (2026). [PMID: 41548739](https://pubmed.ncbi.nlm.nih.gov/41548739/). *American journal of kidney diseases : the official journal of the National Kidney Foundation*. [Case Report / Case Series]
Imai E (2025). [PMID: 39971290](https://pubmed.ncbi.nlm.nih.gov/39971290/). *Internal medicine (Tokyo, Japan)*. [Case Report / Case Series]
Ng YF (2025). [PMID: 41432479](https://pubmed.ncbi.nlm.nih.gov/41432479/). *The Malaysian journal of pathology*. [Case Report / Case Series]
Zhang F (2025). [PMID: 40629285](https://pubmed.ncbi.nlm.nih.gov/40629285/). *BMC nephrology*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Nov 4, 2026, 2:27 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about collagen type III glomerulopathy
Vennavalli NS (2024). [PMID: 39372619](https://pubmed.ncbi.nlm.nih.gov/39372619/). *Indian journal of nephrology*. [Case Report / Case Series]
Ochiai S (2024). [PMID: 38319544](https://pubmed.ncbi.nlm.nih.gov/38319544/). *Journal of nephrology*. [Case Report / Case Series]
Aloudah NM (2024). [PMID: 38662643](https://pubmed.ncbi.nlm.nih.gov/38662643/). *The American journal of case reports*. [Case Report / Case Series]
AI-curated news mentioning collagen type III glomerulopathy
Updated Oct 11, 2026
A study presents four cases of type III collagen deposition glomerulopathy, contributing to the understanding of this rare kidney disease. The findings are summarized alongside a review of existing literature, highlighting the need for further research.
A recent study reports two adult cases of Type III collagen glomerulopathy, highlighting divergent histopathological patterns and potential diagnostic pitfalls. This research contributes to the understanding of this rare kidney disease.