C1q nephropathy in a child with a chromosome 13 deletion

Pediatric Nephrology : Journal of the International Pediatric Nephrology Association
Isabel RobertiDae Un Kim

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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Citations

Oct 24, 2007·Pediatric Nephrology : Journal of the International Pediatric Nephrology Association·Jameela A Kari, Sawsan M Jalalah
Feb 25, 2010·Pediatric Nephrology : Journal of the International Pediatric Nephrology Association·Scott E WenderferMichael C Braun
Apr 18, 2009·Clinical and Experimental Nephrology·Akiko MiiYuh Fukuda

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