Literature DB >> 33413160

Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome.

Qi Chen1, Xiaoyi Wang1, Jingjing Min2, Lin Wang3, Lijun Mou4.   

Abstract

BACKGROUND: Gitelman syndrome (GS) is an autosomal recessive inherited salt-losing tubulopathy (SLT). Here, we describe, for the first time, a case of GS without Gitelman-like features and with concomitant kidney stones, cysts and diabetic nephropathy (DN). CASE
PRESENTATION: We described a male patient had a 19-year history of recurrent fatigue. From childhood, he had polydipsia and polyuria, paroxysmal tetany and palpitation. Serum biochemistry revealed chronic hypokalemia, metabolic alkalosis, normomagnesemia, mildly elevated Cr. Concomitant 24 h urine collection showed inappropriate renal potassium wasting, borderline hypercalciuria, moderate proteinuria consisting of major glomerular. Ultrasound of urinary tract showed bilateral and multiple kidney stones and cysts. Whole exome sequencing (WES) identified compound heterozygous mutations of SLC12A3. The unusual association of SLTs and glomerular proteinuria prompted us to perform a renal biopsy. Renal pathology showed renal involvement consistent with GS and early stage of diabetic nephropathy (DN). After treatment with KCl, magnesium oxide, perindopril and acarbose, the patient had been cured. The fatigue didn't relapse.
CONCLUSION: GS had high variability of phenotype, GS may have no Gitelman-like features, kidney stones are not the exclusion criteria of GS. Renal biopsy should be warranted for GS patients with moderate to massive glomerular proteinuria.

Entities:  

Keywords:  Case report; Diabetic nephropathy; Gitelman syndrome; Kidney stones

Mesh:

Year:  2021        PMID: 33413160      PMCID: PMC7791706          DOI: 10.1186/s12882-020-02211-y

Source DB:  PubMed          Journal:  BMC Nephrol        ISSN: 1471-2369            Impact factor:   2.388


  11 in total

Review 1.  Gitelman's syndrome: a pathophysiological and clinical update.

Authors:  Farid Nakhoul; Nakhoul Nakhoul; Evgenia Dorman; Liron Berger; Karl Skorecki; Daniella Magen
Journal:  Endocrine       Date:  2011-11-15       Impact factor: 3.633

2.  Exonic mutations in the SLC12A3 gene cause exon skipping and premature termination in Gitelman syndrome.

Authors:  Yoichi Takeuchi; Eikan Mishima; Hisato Shima; Yasutoshi Akiyama; Chitose Suzuki; Takehiro Suzuki; Takayasu Kobayashi; Yoichi Suzuki; Tomohiro Nakayama; Yasuhiro Takeshima; Norma Vazquez; Sadayoshi Ito; Gerardo Gamba; Takaaki Abe
Journal:  J Am Soc Nephrol       Date:  2014-07-24       Impact factor: 10.121

3.  Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.

Authors:  Anne Blanchard; Detlef Bockenhauer; Davide Bolignano; Lorenzo A Calò; Etienne Cosyns; Olivier Devuyst; David H Ellison; Fiona E Karet Frankl; Nine V A M Knoers; Martin Konrad; Shih-Hua Lin; Rosa Vargas-Poussou
Journal:  Kidney Int       Date:  2017-01       Impact factor: 10.612

4.  [Expert consensus for the diagnosis and treatment of patients with Gitelman syndrome].

Authors: 
Journal:  Zhonghua Nei Ke Za Zhi       Date:  2017-09-01

5.  Abnormal glucose metabolism and insulin sensitivity in Chinese patients with Gitelman syndrome.

Authors:  Hong Ren; Ling Qin; WeiMing Wang; Jun Ma; Wen Zhang; Ping Yan Shen; Hao Shi; Xiao Li; Nan Chen
Journal:  Am J Nephrol       Date:  2013-01-31       Impact factor: 3.754

6.  Gitelman syndrome and glomerular proteinuria: a link between loss of sodium-chloride cotransporter and podocyte dysfunction?

Authors:  Nathalie Demoulin; Selda Aydin; Jean-Pierre Cosyns; Karin Dahan; Georges Cornet; Ines Auberger; Johannes Loffing; Olivier Devuyst
Journal:  Nephrol Dial Transplant       Date:  2014-09       Impact factor: 5.992

7.  Hydrochlorothiazide Test as a Tool in the Diagnosis of Gitelman Syndrome in Chinese Patients.

Authors:  Xiaoyan Peng; Bingbin Zhao; Lei Zhang; Lanping Jiang; Tao Yuan; Ying Wang; Haiyun Wang; Jie Ma; Naishi Li; Ke Zheng; Min Nie; Xuemei Li; Xiaoping Xing; Limeng Chen
Journal:  Front Endocrinol (Lausanne)       Date:  2018-09-24       Impact factor: 5.555

8.  Glucose tolerance and insulin responsiveness in Gitelman syndrome patients.

Authors:  Tao Yuan; Lanping Jiang; Chen Chen; Xiaoyan Peng; Min Nie; Xuemei Li; Xiaoping Xing; Xuewang Li; Limeng Chen
Journal:  Endocr Connect       Date:  2017-04-21       Impact factor: 3.335

9.  A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene.

Authors:  Qin Chen; Yaqin Wu; Jingya Zhao; Ying Jia; Wei Wang
Journal:  BMC Nephrol       Date:  2018-10-19       Impact factor: 2.388

10.  Arg913Gln variation of SLC12A3 gene is associated with diabetic nephropathy in type 2 diabetes and Gitelman syndrome: a systematic review.

Authors:  Eduardo De la Cruz-Cano; Cristina Del C Jiménez-González; Vicente Morales-García; Conny Pineda-Pérez; Juan G Tejas-Juárez; Francisco J Rendón-Gandarilla; Silvia Jiménez-Morales; José A Díaz-Gandarilla
Journal:  BMC Nephrol       Date:  2019-10-28       Impact factor: 2.388

View more
  3 in total

Review 1.  Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians.

Authors:  Laura Nuñez-Gonzalez; Noa Carrera; Miguel A Garcia-Gonzalez
Journal:  Int J Mol Sci       Date:  2021-10-22       Impact factor: 5.923

2.  A case of Gitelman syndrome with membranous nephropathy.

Authors:  Xiafei Guo; Shanshen Yu; Jia Sun; Lijun Mou
Journal:  BMC Nephrol       Date:  2022-07-26       Impact factor: 2.585

3.  Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes.

Authors:  Ramón Peces; Carlos Peces; Rocío Mena; Emilio Cuesta; Fe Amalia García-Santiago; Marta Ossorio; Sara Afonso; Pablo Lapunzina; Julián Nevado
Journal:  Genes (Basel)       Date:  2022-02-23       Impact factor: 4.096

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.