Literature DB >> 6878256

Hereditary glomerulonephritis of non-Alport type.

C C Doherty, D T Middleton, C M Hill.   

Abstract

In three unrelated kindreds, 21 subjects with hereditary renal disease were identified. The mode of inheritance was autosomal dominant and the main clinical features were asymptomatic proteinuria and/or haematuria. Three of the 16 females but none of the five males developed progressive renal failure. Renal biopsy carried out in six of the 21 patients showed varying degrees of mesangial change with glomerular deposition of IgM and C3 in some cases. Nerve deafness and renal ultrastructural changes typical of Alport's Syndrome were absent. The renal disease in these subjects does not conform with previously recognised types of familial nephropathy.

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Year:  1983        PMID: 6878256

Source DB:  PubMed          Journal:  Proc Eur Dial Transplant Assoc        ISSN: 0071-2736


  2 in total

1.  Long term prognosis of recurrent haematuria.

Authors:  P F Miller; N I Speirs; S R Aparicio; M Lendon; J M Savage; R J Postlethwaite; J T Brocklebank; I B Houston; S R Meadow
Journal:  Arch Dis Child       Date:  1985-05       Impact factor: 3.791

2.  Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study.

Authors:  C Izzi; S Sanna-Cherchi; E Prati; R Belleri; A Remedio; R Tardanico; M Foramitti; S Guerini; B F Viola; E Movilli; I Beerman; R Lifton; L Leone; A Gharavi; F Scolari
Journal:  Kidney Int       Date:  2006-03       Impact factor: 10.612

  2 in total

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