Literature DB >> 2593909

Thin-membrane nephropathy--a common cause of glomerular haematuria.

G J Perry1, C R George, M J Field, P V Collett, S Kalowski, R N Wyndham, R C Newland, B P Lin, K L Kneale, J R Lawrence.   

Abstract

Thin-membrane nephropathy recently has been described as a cause of glomerular haematuria. The prognosis of the condition is unclear but it generally is considered to be benign. In a series of 92 patients with glomerular haematuria, thin-membrane nephropathy was found to be a common cause, occurring in 26 (28%) patients. Sixteen patients were women. The mean age was 42 years. Four patients had a family history of renal disease or haematuria and no patient was deaf. Haematuria had been present from six days to 30 years. Loin pain occurred in 31% of patients. Hypertension was not a feature and mild renal impairment was present in one case only, while a further three cases showed proteinuria at a level of greater than 500 mg of protein per day. Glomerular basement membranes in patients with thin-membrane nephropathy gave a mean (+/- standard deviation) width of 319 + 37 nm which was significantly (P less than 0.002) less than the control value of 394 +/- 61 nm. On the basis of clinical features and serological parameters, thin-membrane nephropathy could not be separated from other renal causes of haematuria but required careful electronmicroscopic examination of renal biopsy material to establish the diagnosis. Limited follow-up has confirmed the good prognosis of the condition.

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Year:  1989        PMID: 2593909     DOI: 10.5694/j.1326-5377.1989.tb139637.x

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  6 in total

1.  Ocular abnormalities in thin basement membrane disease.

Authors:  D Colville; J Savige; P Branley; D Wilson
Journal:  Br J Ophthalmol       Date:  1997-05       Impact factor: 4.638

2.  Nine novel COL4A3 and COL4A4 mutations and polymorphisms identified in inherited membrane diseases.

Authors:  Kesha Rana; Stephen Tonna; Yan Yan Wang; Lydia Sin; Tina Lin; Elizabeth Shaw; Ishanee Mookerjee; Judy Savige
Journal:  Pediatr Nephrol       Date:  2007-01-10       Impact factor: 3.714

3.  Permselectivity in thin membrane nephropathy.

Authors:  D M Thomas; G A Coles; D F Griffiths; J D Williams
Journal:  J Clin Invest       Date:  1994-05       Impact factor: 14.808

4.  Value of urinary excretion of microalbumin in predicting glomerular lesions in children with isolated microscopic hematuria.

Authors:  Farahnak K Assadi
Journal:  Pediatr Nephrol       Date:  2005-06-08       Impact factor: 3.714

Review 5.  Heterozygous Pathogenic COL4A3 and COL4A4 Variants (Autosomal Dominant Alport Syndrome) Are Common, and Not Typically Associated With End-Stage Kidney Failure, Hearing Loss, or Ocular Abnormalities.

Authors:  Judy Savige
Journal:  Kidney Int Rep       Date:  2022-06-07

6.  A Novel COL4A4 Mutation Identified in a Chinese Family with Thin Basement Membrane Nephropathy.

Authors:  Yan Xu; Min Guo; Hui Dong; Wei Jiang; Ruixia Ma; Shiguo Liu; Shenqian Li
Journal:  Sci Rep       Date:  2016-02-02       Impact factor: 4.379

  6 in total

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