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Case Reports in Nephrology
Scopus
ISSN 2090-665X · Wiley · 477 artikel di indeks
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Artikel Jurnal
A Rare NPHS2 Mutation (E130K) in Hereditary Steroid-Resistant Nephrotic Syndrome: A Case Report
Hereditary steroid-resistant nephrotic syndrome (HSRNS) due to mutations in the NPHS2 gene (encoding podocin) is a rare genetic condition that typically presents in childhood. We report a case of a 2-year-and-8-month-old male, the seventh child of consanguineous parents, who presented with…
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Light Chain Deposition Disease and Light Chain Cast Nephropathy in a Patient With Multiple Myeloma and HIV Infection: A Case Report
Kidney dysfunction is a common complication in multiple myeloma (MM), typically presenting with cast nephropathy as a single pattern of injury on kidney biopsy and infrequently occurs in people living with human immunodeficiency virus (PLHIV). A man in his 50s, newly diagnosed with HIV, who was…
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Artikel Jurnal
Is it Always Safe to Administer RAS Inhibitors to Patients Who Underwent Unilateral Radical Nephrectomy?
Compensatory increases in single-kidney glomerular filtration rate (GFR) are usually observed after unilateral radical nephrectomy. However, the influence of hemodynamically active therapies on early functional compensation remains uncertain. We describe a 65-year-old man with latent autoimmune…
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Artikel Jurnal
Type III Collagen Glomerulopathy Presenting With Divergent Histopathological Patterns: Report of Two Adult Cases and Diagnostic Pitfalls
Type III collagen glomerulopathy (collagenofibrotic glomerulopathy) is a rare idiopathic renal disorder. It is characterized by abnormal deposition of Type III collagen fibrils within the mesangial and subendothelial compartments of glomeruli. Due to its nonspecific clinical presentation and…
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Artikel Jurnal
Membranous Nephropathy Secondary to Syphilis
Membranous nephropathy (MN) is one of the most common causes of nephrotic syndrome in the adult population. Although the majority of the cases of MN are without any inciting event, about a third are caused or associated with immune diseases, infectious diseases, and drugs and toxins. There have…
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Artikel Jurnal
Gitelman Syndrome in a Child Presenting With Polyuria and Polydipsia: Diagnostic Challenges in a Resource-Limited Setting
Gitelman syndrome (GS) is a rare inherited renal salt-wasting tubulopathy characterized by hypokalemia, hypomagnesemia, and hypocalciuria. Its nonspecific presentation often overlaps with that of more common pediatric conditions, leading to delayed diagnosis, particularly in resource-limited…
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Artikel Jurnal
Rapidly Progressive IgA Nephropathy in a Patient With a History of Breast Cancer: A Case Report and Literature Review
IgA nephropathy (IgAN), or Berger’s disease, is the most common primary glomerulopathy worldwide. It is characterized by dominant mesangial deposition of immunoglobulin A1 (IgA1), typically of the galactose-deficient form (Gd-IgA1), which triggers the formation of circulating immune complexes and…
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Artikel Jurnal
A Classic and Unusual Presentation of Atheroembolic Renal Disease: Report of Two Cases
Atheroembolic renal disease (AERD) is an underdiagnosed condition with diverse clinical presentations that can mimic various renal pathologies. Most cases follow intravascular procedures or anticoagulation, while only rare case reports of spontaneous AERD have been described. We present two…