ArticlePediatric nephrology (Berlin, Germany)2025
Podocyte infolding glomerulopathy in a school-aged child.
Article in Pediatric nephrology (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Podocyte infolding glomerulopathy in a Japanese girl with systemic lupus erythematosus.CEN case reports · 2026Article
- A comparative study on the efficacy of rituximab combined with tacrolimus and methylprednisolone in the treatment of patients with moderate-high risk idiopathic membranous nephropathy.American journal of translational research · 2026Article
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Authors and funding
6 authors.
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Abstract
backgroundPodocyte infolding glomerulopathy (PIG) is a rare kidney disorder characterized by the infolding of podocyte processes into the glomerular basement membrane. The condition presents with nephrotic syndrome, yet its pathogenesis and clinical implications remain poorly understood due to limited case reports. Most documented cases have originated from Japan, highlighting a significant gap in the literature regarding its prevalence and characteristics in other regions, including the Indian subcontinent. CASE: A 5-year-old boy presented with hypertension, edema, nephrotic range proteinuria, and 3 weeks later developed macroscopic hematuria. Kidney biopsy revealed characteristic microtubule formation within the glomerular basement membrane, confirming the diagnosis of PIG. Initial treatment with prednisolone was unsuccessful, leading to the addition of tacrolimus which resulted in significant improvements in the child's proteinuria and hematuria.
conclusionThis case contributes to the limited literature on PIG and highlights the need for more research to establish standardized treatment protocols.
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