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Updated: Aug 11, 2026

Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
Published on: February 3, 2012
C1q nephropathy in a child with a chromosome 13 deletion
Isabel Roberti1, Sachin Sachdev, Adam Aronsky
1Pediatric Nephrology and Transplantation, East Wing, Suite 304, Saint Barnabas Medical Center, 94 Old Short Hills Road , Livingston, NJ 07039, USA. Iroberti@sbhcs.com
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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