Literature DB >> 16520946

C1q nephropathy in a child with a chromosome 13 deletion.

Isabel Roberti1, Sachin Sachdev, Adam Aronsky, Dae 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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Year:  2006        PMID： 16520946     DOI： 10.1007/s00467-006-0046-1

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


  11 in total

Review 1.  Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint.

Authors:  Martin R Pollak
Journal:  J Am Soc Nephrol       Date:  2002-12       Impact factor: 10.121

2.  C1q nephropathy: a pediatric clinicopathologic study.

Authors:  S S Iskandar; M C Browning; W B Lorentz
Journal:  Am J Kidney Dis       Date:  1991-10       Impact factor: 8.860

3.  Spontaneous improvement in a case of C1q nephropathy.

Authors:  M Nishida; H Kawakatsu; H Komatsu; K Ishiwari; M Tamai; T Sawada
Journal:  Am J Kidney Dis       Date:  2000-05       Impact factor: 8.860

4.  Nonsystemic mesangiopathic glomerulonephritis with "full house" immunofluorescence. Pathological and clinical observation in five patients.

Authors:  E Jones; A Magil
Journal:  Am J Clin Pathol       Date:  1982-07       Impact factor: 2.493

5.  Retinoblastoma and chromosome 13 deletion.

Authors:  A Gencík; P Auf der Maur; A Gencíkova; J Lütschg
Journal:  Helv Paediatr Acta       Date:  1982

6.  Steroid-resistant nephrotic syndrome and congenital anomalies of kidneys: evidence of locus on chromosome 13q.

Authors:  Abhay N Vats; Chandra Ishwad; Kalyani R Vats; Michael Moritz; Demetrius Ellis; Christine Mueller; Urvashi Surti; Maria Z Parizhskaya; Manuel P Meza; Leah Burke; Francis X Schneck; Malika Saxena; Robert Ferrell
Journal:  Kidney Int       Date:  2003-07       Impact factor: 10.612

7.  C1q nephropathy: a variant of focal segmental glomerulosclerosis.

Authors:  Glen S Markowitz; Joshua A Schwimmer; M Barry Stokes; Samih Nasr; Robert L Seigle; Anthony M Valeri; Vivette D D'Agati
Journal:  Kidney Int       Date:  2003-10       Impact factor: 10.612

8.  C1q nephropathy: do C1q deposits have any prognostic significance in the nephrotic syndrome?

Authors:  A Davenport; A G Maciver; J C Mackenzie
Journal:  Nephrol Dial Transplant       Date:  1992       Impact factor: 5.992

9.  C1q nephropathy: a distinct pathologic entity usually causing nephrotic syndrome.

Authors:  J C Jennette; C G Hipp
Journal:  Am J Kidney Dis       Date:  1985-08       Impact factor: 8.860

10.  Survival after retinoblastoma: long-term consequences and family history of cancer.

Authors:  J Byrne; T R Fears; C Whitney; D M Parry
Journal:  Med Pediatr Oncol       Date:  1995-03
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  3 in total

Review 1.  C1q nephropathy in the pediatric population: pathology and pathogenesis.

Authors:  Scott E Wenderfer; Rita D Swinford; Michael C Braun
Journal:  Pediatr Nephrol       Date:  2010-02-24       Impact factor: 3.714

2.  C1q nephropathy in two young sisters.

Authors:  Jameela A Kari; Sawsan M Jalalah
Journal:  Pediatr Nephrol       Date:  2007-10-21       Impact factor: 3.714

Review 3.  Current status and issues of C1q nephropathy.

Authors:  Akiko Mii; Akira Shimizu; Yukinari Masuda; Emiko Fujita; Kaoru Aki; Masamichi Ishizaki; Shigeru Sato; Adam Griesemer; Yuh Fukuda
Journal:  Clin Exp Nephrol       Date:  2009-04-17       Impact factor: 2.801
  3 in total

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