Literature DB >> 860725

Development of the characteristic ultrastructural lesion of hereditary nephritis during the course of the disease.

G A Beathard, N A Granholm.   

Abstract

The diagnosis of hereditary nephritis in the absence of a clear family history or the presence of characteristic ancillary abnormalities is difficult, but it has considerable prognostic importance. The recent recognition of an ultrastructural lesion characteristic of this disease, although not present in all families, is of considerable value. In this report we describe a kindred with the lesion-associated disease that differs from those previously described in that the lesion developed during the course of the disease, was not present in all affected members and appeared to be the result of paternal transmission.

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Year:  1977        PMID: 860725     DOI: 10.1016/0002-9343(77)90878-6

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  1 in total

Review 1.  Alport's syndrome: specificity and pathogenesis of glomerular basement membrane alterations.

Authors:  H J Rumpelt
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

  1 in total

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