Literature DB >> 27904828

Dent's disease complicated by nephrotic syndrome: A case report.

Guohua He1, Hongwen Zhang2, Shanshan Cao3, Huijie Xiao2, Yong Yao2.   

Abstract

Dent's disease is an X-linked recessive proximal tubular disorder that mostly affects male patients in childhood or early adult life. The condition is caused by mutations in the CLCN5 (Dent disease 1) or OCRL (Dent disease 2) genes located on chromosome Xp11.22 and Xq25, respectively. In most male patients, proteinuria is subnephrotic but may reach nephrotic levels. Here, we report the first case of Dent's disease complicated by nephrotic syndrome. Dent's disease should be considered in the differential diagnosis of nephrotic syndrome, and especially in male patients with early onset of nephrotic syndrome. A urinary α1-microglobulin/albumin ratio > 1 may provide the first clue to a tubulopathy.

Entities:  

Keywords:  Dent's disease; OCRL gene; nephrotic syndrome; proteinuria

Year:  2016        PMID: 27904828      PMCID: PMC5116868          DOI: 10.5582/irdr.2016.01058

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  17 in total

1.  Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.

Authors:  A G Norden; S J Scheinman; M M Deschodt-Lanckman; M Lapsley; J L Nortier; R V Thakker; R J Unwin; O Wrong
Journal:  Kidney Int       Date:  2000-01       Impact factor: 10.612

2.  The long-term use of enalapril and hydrochlorothiazide in two novel mutations patients with Dent's disease type 1.

Authors:  Maria Helena Vaisbich; Luciana Dos Santos Henriques; Takashi Igarashi; Takashi Sekine; George Seki; Vera H Koch
Journal:  J Bras Nefrol       Date:  2012-03

Review 3.  Urine retinol-binding protein 4: a functional biomarker of the proximal renal tubule.

Authors:  Anthony G W Norden; Marta Lapsley; Robert J Unwin
Journal:  Adv Clin Chem       Date:  2014       Impact factor: 5.394

4.  X-linked recessive nephrolithiasis with renal failure.

Authors:  P A Frymoyer; S J Scheinman; P B Dunham; D B Jones; P Hueber; E T Schroeder
Journal:  N Engl J Med       Date:  1991-09-05       Impact factor: 91.245

5.  Renal manifestations of Dent disease and Lowe syndrome.

Authors:  Hee Yeon Cho; Bum Hee Lee; Hyun Jin Choi; Il Soo Ha; Yong Choi; Hae Il Cheong
Journal:  Pediatr Nephrol       Date:  2007-11-24       Impact factor: 3.714

6.  Dent disease in children: diagnostic and therapeutic considerations.

Authors:  Maria Szczepanska; Marcin Zaniew; Florian Recker; Malgorzata Mizerska-Wasiak; Iga Zaluska-Lesniewska; Katarzyna Kilis-Pstrusinska; Piotr Adamczyk; Jan Zawadzki; Krzysztof Pawlaczyk; Michael Ludwig; Przemyslaw Sikora
Journal:  Clin Nephrol       Date:  2015-10       Impact factor: 0.975

7.  Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Authors:  Yaacov Frishberg; Dganit Dinour; Ruth Belostotsky; Rachel Becker-Cohen; Choni Rinat; Sofia Feinstein; Paulina Navon-Elkan; Efrat Ben-Shalom
Journal:  Pediatr Nephrol       Date:  2009-12       Impact factor: 3.714

8.  Urinary α1 -microglobulin and albumin excretion in children and adolescents with type 1 diabetes.

Authors:  Aasem Saif; Neveen Soliman
Journal:  J Diabetes       Date:  2016-03-16       Impact factor: 4.006

9.  Twenty-Four-Hour Urine α1 -Microglobulin as a Marker of Hypertension-Induced Renal Impairment and Its Response on Different Blood Pressure-Lowering Drugs.

Authors:  Charalampos I Liakos; Gregory P Vyssoulis; Maria I Markou; Nikolaos V Kafkas; Konstantinos P Toutouzas; Dimitrios Tousoulis
Journal:  J Clin Hypertens (Greenwich)       Date:  2016-03-18       Impact factor: 3.738

Review 10.  The cellular and physiological functions of the Lowe syndrome protein OCRL1.

Authors:  Zenobia B Mehta; Grzegorz Pietka; Martin Lowe
Journal:  Traffic       Date:  2014-03-07       Impact factor: 6.215

View more
  5 in total

1.  Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome.

Authors:  Samuela Landini; Benedetta Mazzinghi; Francesca Becherucci; Marco Allinovi; Aldesia Provenzano; Viviana Palazzo; Fiammetta Ravaglia; Rosangela Artuso; Emanuele Bosi; Stefano Stagi; Giulia Sansavini; Francesco Guzzi; Luigi Cirillo; Augusto Vaglio; Luisa Murer; Licia Peruzzi; Andrea Pasini; Marco Materassi; Rosa Maria Roperto; Hans-Joachim Anders; Mario Rotondi; Sabrina Rita Giglio; Paola Romagnani
Journal:  Clin J Am Soc Nephrol       Date:  2019-12-12       Impact factor: 8.237

2.  A rare case of nephrotic syndrome associated with Dent's disease: a case report.

Authors:  Shinichi Makino; Maulana A Empitu; Toshimasa Naito; Masayoshi Ishii; Hanae Wakabayashi; Chiwei Lee; Masashi Aizawa; Katsuhiko Asanuma
Journal:  CEN Case Rep       Date:  2020-06-12

Review 3.  Nephrocalcinosis: A Review of Monogenic Causes and Insights They Provide into This Heterogeneous Condition.

Authors:  Fay J Dickson; John A Sayer
Journal:  Int J Mol Sci       Date:  2020-01-06       Impact factor: 5.923

4.  Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Authors:  Lisa Gianesello; Jennifer Arroyo; Dorella Del Prete; Giovanna Priante; Monica Ceol; Peter C Harris; John C Lieske; Franca Anglani
Journal:  Genes (Basel)       Date:  2021-10-11       Impact factor: 4.141

Review 5.  Look Alike, Sound Alike: Phenocopies in Steroid-Resistant Nephrotic Syndrome.

Authors:  Francesca Becherucci; Samuela Landini; Luigi Cirillo; Benedetta Mazzinghi; Paola Romagnani
Journal:  Int J Environ Res Public Health       Date:  2020-11-12       Impact factor: 3.390

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.