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  3. Vol. 3 No. 2 (2015): Spring
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Vol. 3 No. 2 (2015)

May 2015

Renal Amyloidosis Due to Juvenile Rheumatoid Arthritis Occurring in Early Childhood

  • Mahmood Maleknejad
  • Jalil Moshari
  • Anosh Azarfar
  • Mohammad Esmaeili
  • Nona Zabolynejad
  • Zahra Rezayi Yazdi
  • Fatemeh Ghane Sharbaf

Journal of Pediatric Nephrology, Vol. 3 No. 2 (2015), 2 May 2015 , Page 79-81
https://doi.org/10.22037/jpn.v3i2.8203 Published: 2015-04-15

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Abstract

Renal amyloidosis is a late manifestation of chronic juvenile rheumatoid arthritis (JRA) and usually manifests during the first 10 to 15 years after the onset of JRA. We hereby report a boy with JRA-related renal amyloidosis who presented with nephrotic syndrome in early childhood. Amyloidosis was associated with a 6-year history of juvenile rheumatic arthritis (JRA). Diagnosis of renal amyloidosis was confirmed by the deposition of Congo red positive amyloid fibrils within the glomeruli. Polarized light microscopy showed the classic green birefringence appearance.

Key words: Arthritis, Juvenile; Amyloidosis, familial renal; Child
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How to Cite

1.
Maleknejad M, Moshari J, Azarfar A, Esmaeili M, Zabolynejad N, Rezayi Yazdi Z, et al. Renal Amyloidosis Due to Juvenile Rheumatoid Arthritis Occurring in Early Childhood. J Ped Nephrol [Internet]. 2015 Apr. 15 [cited 2026 Jul. 8];3(2):79-81. Available from: https://journals.sbmu.ac.ir/jpn/article/view/8203
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References

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