Congenital and Infantile Nephrotic Syndrome in Thai Infants

Author:

Vachvanichsanong Prayong1,Mitarnun Winyou2,Tungsinmunkong Kobkul2,Dissaneewate Pornsak1

Affiliation:

1. Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Hat-Yai, Thailand

2. Department of Pathology, Faculty of Medicine, Prince of Songkla University, Hat-Yai, Thailand

Abstract

Congenital and infantile nephrotic syndrome reported from the Eastern world is rare and might be a different entity from that in the West. In a retrospective review of 10 nephrotic syndrome in Thai infants (5 girls and 5 boys), 7 were diagnosed with congenital nephrotic syndrome and 3 with infantile nephrotic syndrome. Two had congenital nephrotic syndrome secondary to congenital syphilis. All had edema, ascites, and failure to thrive. Of the 3 patients tested for thyroid function, all showed hypothyroidism. Two patients developed renal failure. Renal tissue was examined from 4 patients from 3 biopsies and 2 autopsies; only 1 patient showed tubular microcysts. Symptomatic therapy was performed concurrently with penicillin therapy in 2 patients having congenital syphilis. Prednisolone, cyclophosphamide, captopril, and enalapril were tried in some patients, with little effect. Five patients died from respiratory failure complicated by later infection, 1 patient died from renal failure, and 4 patients were lost to follow-up. Nephrotic syndrome in the first year of life in the Eastern world is rare. Prognosis of nephrotic syndrome in Thai infants at this time is still poor.

Publisher

SAGE Publications

Subject

Pediatrics, Perinatology and Child Health

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