A clinicopathologic study of forty-eight infants with nephrotic syndrome

R. K. Sibley, J. Mahan, S. M. Mauer, R. L. Vernier

Research output: Contribution to journalArticlepeer-review

60 Scopus citations


The clinical and histopathologic features of 48 children presenting with the nephrotic syndrome during the first year of life were analyzed. Proteinuria was discovered soon after birth to 3 months of age in 39 infants (congenital nephrotic syndrome), and nine infants had an infantile onset presenting between 4 and 12 months of age. Neither histologic parameters - microglomeruli, epithelial, or mesangial proliferation, focal segmental or global sclerosis, fibrinoid necrosis, or tubular microcysts - nor histologic classification - microcystic disease, mesangial proliferative glomerulonephritis, focal segmental glomerular sclerosis/hyalinosis-predicted the outcome. Rather, age at presentation was found to predict outcome: One of 39 infants with a congenital onset and seven of nine infants with an infantile onset underwent a complete remission (P < 0.0001).

Original languageEnglish (US)
Pages (from-to)544-552
Number of pages9
JournalKidney international
Issue number3
StatePublished - 1985


Dive into the research topics of 'A clinicopathologic study of forty-eight infants with nephrotic syndrome'. Together they form a unique fingerprint.

Cite this