Literature DB >> 10975308

Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases.

I H Su1, R Frank, B G Gauthier, E Valderrama, D B Simon, R P Lifton, H Trachtman.   

Abstract

We describe a patient with signs and symptoms of classic Bartter syndrome. The patient tested negative for all known genetic abnormalities associated with this tubular disorder. Proteinuria was found within 1 year after the diagnosis of Bartter syndrome. A renal biopsy performed 6 months later, when her kidney function was normal, revealed focal segmental glomerulosclerosis (FSGS). We propose a link between stimulation of the renin-angiotensin system and sclerotic changes in the glomerulus. This lesion may explain previous reports of kidney failure in patients with Bartter syndrome.

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Year:  2000        PMID： 10975308     DOI： 10.1007/s004670050054

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


  20 in total

1.  A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5.

Authors:  Takayuki Okamoto; Toshihiro Tajima; Tomoya Hirayama; Satoshi Sasaki
Journal:  Eur J Pediatr       Date:  2011-09-20       Impact factor: 3.183

Review 2.  Understanding Bartter syndrome and Gitelman syndrome.

Authors:  Oliver T Fremont; James C M Chan
Journal:  World J Pediatr       Date:  2012-01-27       Impact factor: 2.764

3.  Chronic renal failure in a boy with classic Bartter's syndrome due to a novel mutation in CLCNKB coding for the chloride channel.

Authors:  Chien-Ming Lin; Jeng-Daw Tsai; Yi-Fen Lo; Ming-Tso Yan; Sung-Sen Yang; Shih-Hua Lin
Journal:  Eur J Pediatr       Date:  2008-12-03       Impact factor: 3.183

Review 4.  Salt-Losing Tubulopathies in Children: What's New, What's Controversial?

Authors:  Robert Kleta; Detlef Bockenhauer
Journal:  J Am Soc Nephrol       Date:  2017-12-13       Impact factor: 10.121

5.  A patient with nephrotic-range proteinuria and focal global glomerulosclerosis.

Authors:  Fernando C Fervenza
Journal:  Clin J Am Soc Nephrol       Date:  2013-07-25       Impact factor: 8.237

6.  C1q nephropathy in association with Gitelman syndrome: a case report.

Authors:  Coral Hanevold; Ayesa Mian; Rory Dalton
Journal:  Pediatr Nephrol       Date:  2006-09-06       Impact factor: 3.714

7.  A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis.

Authors:  Ipek Akil; Serkan Ozen; Ali Riza Kandiloglu; Betul Ersoy
Journal:  Clin Exp Nephrol       Date:  2010-02-04       Impact factor: 2.801

Review 8.  Bartter syndrome complicated by immune complex nephropathy. Case report and literature review.

Authors:  Yahya Sardani; Kenan Qin; Mark Haas; Andrew J Aronson; Robert L Rosenfield
Journal:  Pediatr Nephrol       Date:  2003-06-26       Impact factor: 3.714

9.  Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.

Authors:  Hajime Yamazaki; Kandai Nozu; Ichiei Narita; Michio Nagata; Yoshimi Nozu; Xue Jun Fu; Masafumi Matsuo; Kazumoto Iijima; Fumitake Gejyo
Journal:  Pediatr Nephrol       Date:  2008-10-02       Impact factor: 3.714

10.  Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements.

Authors:  Miriam R Berry; Caroline Robinson; Fiona E Karet Frankl
Journal:  Nephrol Dial Transplant       Date:  2013-01-17       Impact factor: 5.992
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