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. 2010 Apr;20(2):68-71.
doi: 10.4103/0971-4065.65297.

Clinical and laboratory findings and therapeutic responses in children with nephrotic syndrome

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Clinical and laboratory findings and therapeutic responses in children with nephrotic syndrome

A A S L Safaei et al. Indian J Nephrol. 2010 Apr.

Retraction in

  • Retraction notice.
    [No authors listed] [No authors listed] Indian J Nephrol. 2011 Jan;21(1):9. Indian J Nephrol. 2011. PMID: 21655162 Free PMC article. No abstract available.

Abstract

Nephrotic syndrome (NS) is a clinical entity characterized by massive loss of urinary protein leading to hypoproteinemia and edema. This prospective cross sectional study was performed on 44 children with idiopathic nephrotic syndrome (INS). The objectives were to study the clinical and biochemical parameters at the time of diagnosis of nephrotic syndrome and to study the histopathological distribution of different subtypes of INS and drug response pattern. There were 29 (66%) males and 15 females (34%). The mean age of NS was 4.87±3.24 years. Facial edema was found in 42 (95%), microscopic hematuria in 10 (23%), gross hematuria in 2 (4.5%), and hypertension in 5 (11.2%) of patients. In 17 children who underwent biopsy, focal segmental glomerulosclerosis was the most common pathologic finding (41%). Other subtypes included minimal change in three (18%), membranoproliferative glomerulonephritis in 1(5.8%), diffuse proliferative glomerulonephritis in 2 (11.6%), membranous glomerulonephritis in 1 (5.8%), and diffuse mesangial proliferation in 3 (17.5%) of cases. At the time of hospital admission, peritonitis were present in five (11.4%), pneumonia and upper respiratory infection (sinusitis) in eight (18%), cellulitis in two (4.5%). Among 44 children with NS, 29 (66%) were steroid sensitive cases, nine (20.5%) were steroid resistant and six (13.5%) were steroid dependent. Among patients with steroid sensitive NS, 37% were without relapsers, 38.8% frequent relapsers and 26.4% were infrequent relapsers. These results suggest that there are differences between season of incidence, response to treatment with corticosteroid and pathologic findings in our study and other studies in Iran and other countries.

Keywords: Children; complication; corticosteroid; nephrotic syndrome; pathology.

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Conflict of interest statement

Conflict of Interest: None declared.

References

    1. Niaudet P. Steroid-sensitive idiopathic nephrotic syndrome. In: Avner ED, Harmon WE, Niaudet P, editors. Pediatric Nephrology. 5th ed. Philadelphia: Lippincott Williams and Wilkins; 2004. pp. 545–73.
    1. Burgstein JM. Nephrotic syndrome. In: Behrman RE, Kliegman RM, Jenson HB, editors. Nelson Textbook of Pediatrics. 18th ed. Philadelphia: Saunders WB; 2008. pp. 2430–42.
    1. Churg J, Habib R, White R. Pathology of the nephrotic symdrome in children.A report from the International Study of Kidney Disease in children. Lancet. 1970;5:1799–802. - PubMed
    1. Falk JR, Jennette JC, Nachman PH. Primary glomerular disease. In: Brenner BM, Levine SA, editors. The Kidney. 7th ed. Philadelphia: Saunders WB; 2004. pp. 1295–307.
    1. Hawkins P. Nephrotic Syndrome. In: Millan JA, Angelis CD, Feigin RD, editors. Oski pediatrics principles and practice. 3rd ed. Philadelphia: Lippincott Williams and Wilkings; 2000. pp. 1590–9.

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