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Case Reports
. 2006 May;21(5):737-9.
doi: 10.1007/s00467-006-0046-1. Epub 2006 Mar 7.

C1q nephropathy in a child with a chromosome 13 deletion

Isabel Roberti  1 , Sachin Sachdev, Adam Aronsky, Dae Un Kim
Affiliations
Case Reports

C1q nephropathy in a child with a chromosome 13 deletion

Isabel Roberti et al. Pediatr Nephrol. 2006 May.

Abstract

C1q nephropathy (C1qNP) is a rare cause of childhood nephrotic syndrome (NS). We describe a child with retinoblastoma, lipomyelomeningocele and a chromosome 13 deletion who presented with massive proteinuria due to C1qNP. Despite steroid resistance, successful treatment of the NS was achieved with mycophenolate mofetil.

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References

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