Literature DB >> 23775203

Nephrotic range proteinuria as a presenting feature of classical nephropathic cystinosis.

Gurdeep Singh Dhooria1, Harmesh Singh Bains.   

Abstract

Patients with renal tubular acidosis (RTA) usually have tubular or low molecular weight proteinuria. The authors present a rare case of a 6-y-old girl with Fanconi syndrome secondary to cystinosis, who at presentation had nephrotic range proteinuria along with rickets and failure to thrive. Although hypoalbuminemia and massive proteinuria are characteristics of nephrotic syndrome, there are other conditions which can present with massive proteinuria.

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Year:  2013        PMID: 23775203     DOI: 10.1007/s12098-013-1084-x

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  8 in total

1.  Focal segmental glomerulosclerosis, proteinuria and nephrocalcinosis associated with renal tubular acidosis.

Authors:  Rasheed A Balogun; Nancy D Adams; Joseph Palmisano; Harold Yamase; Irfans Chughtai; Andre A Kaplan
Journal:  Nephrol Dial Transplant       Date:  2002-02       Impact factor: 5.992

2.  An unusual association of primary focal and segmental glomerulosclerosis, distal renal tubular acidosis and secondary erythrocytosis.

Authors:  Manjusha Yadla; Sandeep Reddy; P Sriramnaveen; C Krishnakishore; V V Sainaresh; V Sivakumar
Journal:  Saudi J Kidney Dis Transpl       Date:  2011-09

Review 3.  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 4.  Nephropathic cystinosis: late complications of a multisystemic disease.

Authors:  Galina Nesterova; William Gahl
Journal:  Pediatr Nephrol       Date:  2008-06       Impact factor: 3.714

5.  Late-onset nephropathic cystinosis: clinical presentation, outcome, and genotyping.

Authors:  Aude Servais; Vincent Morinière; Jean-Pierre Grünfeld; Laure-Hélène Noël; Jean-Michel Goujon; Bernadette Chadefaux-Vekemans; Corinne Antignac
Journal:  Clin J Am Soc Nephrol       Date:  2008-01       Impact factor: 8.237

6.  Absence of hypoalbuminemia despite massive proteinuria in focal segmental glomerulosclerosis secondary to hyperfiltration.

Authors:  M Praga; E Morales; J C Herrero; A Pérez Campos; B Domínguez-Gil; R Alegre; J Vara; M A Martínez
Journal:  Am J Kidney Dis       Date:  1999-01       Impact factor: 8.860

7.  Nephrotic proteinuria without hypoalbuminemia: clinical characteristics and response to angiotensin-converting enzyme inhibition.

Authors:  M Praga; B Borstein; A Andres; J Arenas; A Oliet; C Montoyo; L M Ruilope; J L Rodicio
Journal:  Am J Kidney Dis       Date:  1991-03       Impact factor: 8.860

8.  Medullary nephrocalcinosis, distal renal tubular acidosis and polycythaemia in a patient with nephrotic syndrome.

Authors:  Suneth Karunarathne; Yapa Udayakumara; Dumitha Govindapala; Harshini Fernando
Journal:  BMC Nephrol       Date:  2012-07-26       Impact factor: 2.388

  8 in total
  1 in total

1.  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
  1 in total

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