Literature DB >> 7320813

The glomerular basal lamina in hereditary nephritis.

N Yoshikawa, A H Cameron, R H White.   

Abstract

Characteristic ultrastructural alterations of the glomerular basal lamina have been reported in hereditary nephritis. The basal lamina is irregularly thickened and the lamina densa shows replication with a "basket weave" pattern, enclosing electron-lucent lacunae which frequently contain small dense particles. However there is controversy regarding the specificity of this lesion in hereditary nephritis. To determine the specificity, 366 renal biopsies from 310 children were studied retrospectively. Twenty-four out of 27 patients with hereditary nephritis showed the characteristic changes of the basal lamina and they were widespread in 17. Two patients with recurrent haematuria but no family history of deafness or haematuria showed similar extensive changes and are regarded as new mutant cases of hereditary nephritis. Similar changes were seen in 17 of the 281 patients with other conditions but were always localized to a few capillary loops. We conclude that a widespread "basket weave" pattern appears to be confined to hereditary nephritis and is seen in the great majority of such cases.

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Mesh:

Year:  1981        PMID: 7320813     DOI: 10.1002/path.1711350305

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  14 in total

Review 1.  Alport syndrome, basement membranes and collagen.

Authors:  C E Kashtan; M M Kleppel; R J Butkowski; A F Michael; A J Fish
Journal:  Pediatr Nephrol       Date:  1990-09       Impact factor: 3.714

Review 2.  The investigation of haematuria.

Authors:  R H White
Journal:  Arch Dis Child       Date:  1989-01       Impact factor: 3.791

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.  Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis.

Authors:  C Kashtan; A J Fish; M Kleppel; K Yoshioka; A F Michael
Journal:  J Clin Invest       Date:  1986-10       Impact factor: 14.808

Review 5.  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

6.  The effect of aldosterone blockade in patients with Alport syndrome.

Authors:  Hiroshi Kaito; Kandai Nozu; Kazumoto Iijima; Koichi Nakanishi; Kunihiko Yoshiya; Kyoko Kanda; Rafal Przybyslaw Krol; Norishige Yoshikawa; Masafumi Matsuo
Journal:  Pediatr Nephrol       Date:  2006-10-13       Impact factor: 3.714

7.  Glomerular basement membrane thickness in primary diffuse IgA nephropathy: ultrastructural morphometric analysis.

Authors:  M Danilewicz; M Wagrowska-Danilewicz
Journal:  Int Urol Nephrol       Date:  1998       Impact factor: 2.370

8.  Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

Authors:  J A Govan
Journal:  Br J Ophthalmol       Date:  1983-08       Impact factor: 4.638

9.  Glomerular basement membrane abnormalities in infants with heavy proteinuria.

Authors:  K P Mehta; U S Ali; A R Chitale; U Jha; S Khubchandani
Journal:  Pediatr Nephrol       Date:  1993-08       Impact factor: 3.714

Review 10.  Molecular aspects of Alport's syndrome.

Authors:  M Weber; K O Netzer; O Pullig
Journal:  Clin Investig       Date:  1992-09
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