Glomerular Diseases

Glomerular disease can result from many inherited or acquired disorders and can manifest in a variety of ways, ranging in severity from asymptomatic urinary abnormalities to acute kidney injury (AKI) or end-stage renal disease. A kidney biopsy is often required to secure the underlying diagnosis in a patient with suspected Glomerular disease, particularly in patients with nephrotic syndrome or suspected Glomerulonephritis. Rarely, a biopsy cannot be performed or is not needed to secure a diagnosis.

  • Track 1-1 Malarial Nephrolpathy
  • Track 2-2 Nephrotic Syndrome
  • Track 3-3 Acute post-streptococcal glomerulonephritis
  • Track 4-4 Glomerulopathy secondary to virus infection
  • Track 5-5 Acute Nephritis
  • Track 6-6 Rapidly progressive glomerulonephritis
  • Track 7-7 Asymptomatic urinary abnormality
  • Track 8-8 Fabry Disease
  • Track 9-9 Glomerulosclerosis
  • Track 10-10 Focal Segmental Glomerulosclerosis
  • Track 11-11 Minimal Change Disease
  • Track 12-12 Membranous Glomerulonephritis
  • Track 13-13 HIV Associated Nephropathy
  • Track 14-14 Membranoproliferative Glomerulonephritis
  • Track 15-15 Crescentic Glomerulonephritis
  • Track 16-16 Mesangial Proliferative Glomerulonephritis

Related Conference of Nephrology