Literature DB >> 24810952

Expanding the phenotype of proteinuria in Dent disease. A case series.

Monica T Cramer1, Jennifer R Charlton, Agnes B Fogo, Sahar A Fathallah-Shaykh, David J Askenazi, Lisa M Guay-Woodford.   

Abstract

BACKGROUND: Dent disease is an X-linked recessive renal tubular disorder characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and progressive renal failure (MIM 300009). A recent case series identified four patients with CLCN5 mutations who presented with nephrotic-range proteinuria, histologic evidence of focal segmental and/or global sclerosis, and low molecular weight proteinuria. CASE-DIAGNOSIS/TREATMENT: We characterize the clinical, genetic, and histopathological features of seven unrelated adolescent males with nephrotic-range proteinuria and CLCN5 mutations. Six patients underwent renal biopsy prior to assessing tubular proteinuria. All biopsied patients had either segmental sclerosis (3/6) or segmental increase in mesangial matrix (3/6). Five patients revealed some degree of foot process effacement, but only one patient biopsy revealed >50 % foot process effacement. The attenuated foot process effacement suggests the glomerulosclerosis is not due to a primary podocytopathy.
CONCLUSIONS: These data suggest that clinicians should consider a diagnostic evaluation for Dent disease in young males presenting with high-grade proteinuria.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24810952     DOI: 10.1007/s00467-014-2824-5

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


  10 in total

1.  ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

Authors:  N Piwon; W Günther; M Schwake; M R Bösl; T J Jentsch
Journal:  Nature       Date:  2000-11-16       Impact factor: 49.962

Review 2.  X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations.

Authors:  S J Scheinman
Journal:  Kidney Int       Date:  1998-01       Impact factor: 10.612

Review 3.  Receptor-mediated endocytosis in kidney proximal tubules: recent advances and hypothesis.

Authors:  V Marshansky; S Bourgoin; I Londoño; M Bendayan; B Maranda; P Vinay
Journal:  Electrophoresis       Date:  1997-12       Impact factor: 3.535

4.  Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

Authors:  S E Lloyd; S H Pearce; W Günther; H Kawaguchi; T Igarashi; T J Jentsch; R V Thakker
Journal:  J Clin Invest       Date:  1997-03-01       Impact factor: 14.808

5.  Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.

Authors:  Bugsu Ovunc; Edgar A Otto; Virginia Vega-Warner; Pawaree Saisawat; Shazia Ashraf; Gokul Ramaswami; Hanan M Fathy; Dominik Schoeb; Gil Chernin; Robert H Lyons; Engin Yilmaz; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2011-09-08       Impact factor: 10.121

Review 6.  Chloride channels and endocytosis: new insights from Dent's disease and ClC-5 knockout mice.

Authors:  Olivier Devuyst; François Jouret; Céline Auzanneau; Pierre J Courtoy
Journal:  Nephron Physiol       Date:  2005

7.  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

8.  Hypothesis: Dent disease is an underrecognized cause of focal glomerulosclerosis.

Authors:  Lawrence Copelovitch; Martin A Nash; Bernard S Kaplan
Journal:  Clin J Am Soc Nephrol       Date:  2007-08-08       Impact factor: 8.237

9.  Effect of hydrochlorothiazide on urinary calcium excretion in dent disease: an uncontrolled trial.

Authors:  Anne Blanchard; Rosa Vargas-Poussou; Severine Peyrard; Agnes Mogenet; Veronique Baudouin; Bernard Boudailliez; Marina Charbit; George Deschesnes; Nadia Ezzhair; Chantal Loirat; Marie-Alice Macher; Patrick Niaudet; Michel Azizi
Journal:  Am J Kidney Dis       Date:  2008-10-30       Impact factor: 8.860

10.  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

  10 in total
  11 in total

1.  "It's In Your Genes": Exome Sequencing Enables Precision Diagnostics in Proteinuric Kidney Diseases.

Authors:  Franz Schaefer
Journal:  Clin J Am Soc Nephrol       Date:  2019-12-12       Impact factor: 8.237

2.  A Novel CLCN5 Splice Site Mutation in a Boy with Incomplete Phenotype of Dent Disease.

Authors:  Maria Bitsori; Eleni Vergadi; Emmanouil Galanakis
Journal:  J Pediatr Genet       Date:  2019-06-04

3.  Diagnosis and treatment of Dent disease in 10 Chinese boys.

Authors:  Guohua He; Hongwen Zhang; Fang Wang; Xiaoyu Liu; Huijie Xiao; Yong Yao
Journal:  Intractable Rare Dis Res       Date:  2017-02

4.  The ratio of urinary α1-microglobulin to microalbumin can be used as a diagnostic criterion for tubuloproteinuria.

Authors:  Hongwen Zhang; Fang Wang; Huijie Xiao; Yong Yao
Journal:  Intractable Rare Dis Res       Date:  2018-02

Review 5.  The expanding phenotypic spectra of kidney diseases: insights from genetic studies.

Authors:  Marijn F Stokman; Kirsten Y Renkema; Rachel H Giles; Franz Schaefer; Nine V A M Knoers; Albertien M van Eerde
Journal:  Nat Rev Nephrol       Date:  2016-07-04       Impact factor: 28.314

Review 6.  Kidney disease in children: latest advances and remaining challenges.

Authors:  John F Bertram; Stuart L Goldstein; Lars Pape; Franz Schaefer; Rukshana C Shroff; Bradley A Warady
Journal:  Nat Rev Nephrol       Date:  2016-02-01       Impact factor: 28.314

7.  Nephrotic-range Albuminuria as the presenting symptom of Dent-2 disease.

Authors:  Chiara De Mutiis; Andrea Pasini; Claudio La Scola; Fabrizio Pugliese; Giovanni Montini
Journal:  Ital J Pediatr       Date:  2015-06-25       Impact factor: 2.638

8.  The Spectrum of Kidney Diseases in Children Associated with Low Molecular Weight Proteinuria.

Authors:  Shpetim Salihu; Katerina Tosheska; Natasa Aluloska; Zoran Gucev; Svetlana Cekovska; Velibor Tasic
Journal:  Open Access Maced J Med Sci       Date:  2018-05-16

9.  A Novel CLCN5 Mutation Associated With Focal Segmental Glomerulosclerosis and Podocyte Injury.

Authors:  Ashish K Solanki; Ehtesham Arif; Thomas Morinelli; Robert C Wilson; Gary Hardiman; Peifeng Deng; John M Arthur; Juan Cq Velez; Deepak Nihalani; Michael G Janech; Milos N Budisavljevic
Journal:  Kidney Int Rep       Date:  2018-06-18

Review 10.  Proteinuria in Dent disease: a review of the literature.

Authors:  Youri van Berkel; Michael Ludwig; Joanna A E van Wijk; Arend Bökenkamp
Journal:  Pediatr Nephrol       Date:  2016-10-18       Impact factor: 3.714

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.