Literature DB >> 20306297

Acquired Gitelman's syndrome: an oxymoron?

Renu Bansal1, Vinay K Ranga.   

Abstract

We present the case of a 27-year-old woman with end stage renal disease from Diabetes Mellitus type 1 who had been on hemodialysis for a year. Her father, who was otherwise healthy, was evaluated as a possible living donor. Incidentally, during the workup process, he was identified as having Gitelman's syndrome (GS). The transplant proceeded without any complications, following which the recipient developed biochemical abnormalities consistent with GS. Both donor and recipient are doing well at this time. To our knowledge, this is the only known case of kidney donation by a patient with GS either living or deceased.

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Year:  2010        PMID: 20306297     DOI: 10.1007/s11255-010-9727-6

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN: 0301-1623            Impact factor:   2.370


  12 in total

1.  Gitelman's not-so-benign syndrome.

Authors:  Roman T Pachulski; Fernando Lopez; Rashid Sharaf
Journal:  N Engl J Med       Date:  2005-08-25       Impact factor: 91.245

2.  Abnormal reabsorption of Na+/CI- by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome.

Authors:  G Colussi; G Rombolà; C Brunati; M E De Ferrari
Journal:  Am J Nephrol       Date:  1997       Impact factor: 3.754

3.  Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

Authors:  D N Cruz; A J Shaer; M J Bia; R P Lifton; D B Simon
Journal:  Kidney Int       Date:  2001-02       Impact factor: 10.612

Review 4.  Novel NCCT gene mutations as a cause of Gitelman's syndrome and a systematic review of mutant and polymorphic NCCT alleles.

Authors:  Annette Reissinger; Michael Ludwig; Boris Utsch; Astrid Prömse; Johannes Baulmann; Burkhard Weisser; Hans Vetter; Herbert J Kramer; Dirk Bokemeyer
Journal:  Kidney Blood Press Res       Date:  2002       Impact factor: 2.687

5.  Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

Authors:  Melanie Peters; Nikola Jeck; Stephan Reinalter; Andreas Leonhardt; Burkhard Tönshoff; G ünter Klaus G; Martin Konrad; Hannsjörg W Seyberth
Journal:  Am J Med       Date:  2002-02-15       Impact factor: 4.965

6.  Possible discrimination of Gitelman's syndrome from Bartter's syndrome by renal clearance study: report of two cases.

Authors:  T Tsukamoto; T Kobayashi; K Kawamoto; M Fukase; K Chihara
Journal:  Am J Kidney Dis       Date:  1995-04       Impact factor: 8.860

Review 7.  Bartter's and Gitelman's syndromes: from gene to clinic.

Authors:  Maarten Naesens; Paul Steels; René Verberckmoes; Yves Vanrenterghem; Dirk Kuypers
Journal:  Nephron Physiol       Date:  2004

8.  Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Authors:  D B Simon; C Nelson-Williams; M J Bia; D Ellison; F E Karet; A M Molina; I Vaara; F Iwata; H M Cushner; M Koolen; F J Gainza; H J Gitleman; R P Lifton
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

9.  Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter.

Authors:  Shih-Hua Lin; Nai-Lin Cheng; Yu-Juei Hsu; Mitchell L Halperin
Journal:  Am J Kidney Dis       Date:  2004-02       Impact factor: 8.860

10.  Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes.

Authors:  A Bettinelli; M G Bianchetti; E Girardin; A Caringella; M Cecconi; A C Appiani; L Pavanello; R Gastaldi; C Isimbaldi; G Lama
Journal:  J Pediatr       Date:  1992-01       Impact factor: 4.406

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  3 in total

1.  Long-term Clinical Course after Living Kidney Donation by a Patient with Gitelman Syndrome Harboring a Compound Heterozygous Mutation of the SLC12A3 Gene.

Authors:  Sahoko Kamejima; Izumi Yamamoto; Akiko Tajiri; Yudo Tanno; Ichiro Ohkido; Takashi Yokoo
Journal:  Intern Med       Date:  2020-12-15       Impact factor: 1.271

2.  Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation.

Authors:  Takeshi Kusuda; Tadashi Hosoya; Takayasu Mori; Katsuhito Ihara; Hidenori Nishida; Motoko Chiga; Eisei Sohara; Tatemitsu Rai; Ryuji Koike; Shinichi Uchida; Hitoshi Kohsaka
Journal:  Intern Med       Date:  2016-11-01       Impact factor: 1.271

Review 3.  Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review.

Authors:  Xiangchen Gu; Zheling Su; Min Chen; Yanqiu Xu; Yi Wang
Journal:  Nephrology (Carlton)       Date:  2017-08       Impact factor: 2.506

  3 in total

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