Literature DB >> 2253248

Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndrome.

A J Barakat1, P Arianas, A D Glick, M G Butler.   

Abstract

We report a 6-year-old white male with Laurence-Moon-Biedl syndrome and focal sclerosing glomerulonephritis (FSGN). To our knowledge, FSGN has not been reported previously in patients with this syndrome. We wish to alert the clinician to the wide variety of renal abnormalities that can be seen in patients with this rare, autosomal recessive disorder.

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Year:  1990        PMID: 2253248      PMCID: PMC6697078     

Source DB:  PubMed          Journal:  Child Nephrol Urol        ISSN: 1012-6694


  4 in total

Review 1.  Therapeutic targets in focal and segmental glomerulosclerosis.

Authors:  Peter J Lavin; Rasheed Gbadegesin; Tirupapuliyur V Damodaran; Michelle P Winn
Journal:  Curr Opin Nephrol Hypertens       Date:  2008-07       Impact factor: 2.894

2.  A case report: Familial glucocorticoid deficiency associated with familial focal segmental glomerulosclerosis.

Authors:  Nanik Ram; Ali Asghar; Najmul Islam
Journal:  BMC Endocr Disord       Date:  2012-12-11       Impact factor: 2.763

Review 3.  Ciliopathies: an expanding disease spectrum.

Authors:  Aoife M Waters; Philip L Beales
Journal:  Pediatr Nephrol       Date:  2011-01-06       Impact factor: 3.714

4.  Serum C3 and Renal Outcome in Patients with Primary Focal Segmental Glomerulosclerosis.

Authors:  Jian Liu; Jingyuan Xie; Xiaoyan Zhang; Jun Tong; Xu Hao; Hong Ren; Weiming Wang; Nan Chen
Journal:  Sci Rep       Date:  2017-06-22       Impact factor: 4.379

  4 in total

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