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1. C1q nephropathy in a child with a chromosome 13 deletion.

Author

Roberti, Isabel, Sachdev, Sachin, Aronsky, Adam, and Dae Un Kim

Subjects
*NEPHROTIC syndrome in children, *RETINOBLASTOMA, *PROTEINURIA, *PEDIATRIC nephrology, *KIDNEY diseases
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. [ABSTRACT FROM AUTHOR]

Published
2006
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