Answers are grounded in this paper and cite their sources.
Conclusion:CG is a rare disorder characterized by abnormal glomerular deposition of type III collagen.Its cause and pathogenesis are unclear and lack definitive treatment.There is a paucity of cases describing recurrence post-transplant and its implication on long term graft outcomes is unknown.Here, we describe a case of late recurrent CG, presenting with sub-nephrotic proteinuria and stable allograft function.
No takes yet. Share an insight, caveat, or question.
A 2024 study studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: