Literature DB >> 15880329

Thin basement membrane nephropathy associated with other glomerular diseases.

Suzanne M Norby1, Fernando G Cosio.   

Abstract

Many reports confirm that thin basement membrane nephropathy (TBMN) commonly occurs together with other glomerular diseases such as minimal change glomerulonephritis, diabetes, membranous nephropathy, immunoglobulin (Ig)A glomerulonephritis, and focal segmental glomerulosclerosis. We postulate 3 explanations for these observations. The association of minimal change glomerulonephritis with TBMN probably is artifactual whereas the association with diabetes and membranous glomerulonephritis probably is coincidental. However, the link between TBMN and IgA disease and focal segmental glomerulosclerosis may be pathogenetic. Clinical evidence indicates that the presence of an associated glomerulopathy significantly worsens the prognosis of TBMN. Thus, patients with TBMN and another glomerular lesion usually have more marked proteinuria, and are more likely to have hypertension and renal insufficiency. The frequency of another glomerulopathy in patients with TBMN means that all patients in whom TBMN is suspected but who have heavy proteinuria or renal insufficiency should undergo a renal biopsy examination. However, there is no evidence that TBMN alters the prognosis of another glomerulopathy, and, in particular, patients with TBMN and IgA disease do not have different clinical features or a worse prognosis than those with IgA disease alone.

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Year:  2005        PMID: 15880329     DOI: 10.1016/j.semnephrol.2005.01.010

Source DB:  PubMed          Journal:  Semin Nephrol        ISSN: 0270-9295            Impact factor:   5.299


  10 in total

1.  Thin basement membrane nephropathy associated with minimal change disease in a 15-year-old boy.

Authors:  Shuichiro Fujinaga; Kazunari Kaneko; Yoshiyuki Ohtomo; Hitohiko Murakami; Mayako Takemoto; Masaru Takada; Toshiaki Shimizu; Yuichiro Yamashiro
Journal:  Pediatr Nephrol       Date:  2005-12-17       Impact factor: 3.714

2.  Pattern of double glomerulopathy in children.

Authors:  Hae Il Cheong; Hee Yeon Cho; Kyung Chul Moon; Il Soo Ha; Yong Choi
Journal:  Pediatr Nephrol       Date:  2006-11-16       Impact factor: 3.714

3.  Pathologic glomerular characteristics and glomerular basement membrane alterations in biopsy-proven thin basement membrane nephropathy.

Authors:  Yusuke Kajimoto; Yoko Endo; Mika Terasaki; Shinobu Kunugi; Toru Igarashi; Akiko Mii; Yasuhiro Terasaki; Akira Shimizu
Journal:  Clin Exp Nephrol       Date:  2019-01-28       Impact factor: 2.801

4.  Correlates of hematuria on glomerular histology and electron microscopy in IgA nephropathy.

Authors:  Rohit Tewari; Ritambhra Nada; Maninder Kaur; Puja Dudeja; Charan Singh Rayat; Vinay Sakhuja; Kusum Joshi
Journal:  Med J Armed Forces India       Date:  2016-03-29

Review 5.  Lupus nephritis and thin glomerular basement membrane coexistence: case report and review of the literature.

Authors:  Adriana Acosta; David Arroyo; Francisco Javier Díaz-Crespo; Marian Goicoechea
Journal:  Int Urol Nephrol       Date:  2021-07-15       Impact factor: 2.370

Review 6.  The role of molecular genetics in diagnosing familial hematuria(s).

Authors:  Constantinos Deltas; Alkis Pierides; Konstantinos Voskarides
Journal:  Pediatr Nephrol       Date:  2011-06-19       Impact factor: 3.714

7.  Co-existence of thin basement membrane nephropathy with other glomerular pathologies; a single center experience.

Authors:  Rizwan A Qazi; Bahar Bastani
Journal:  J Nephropathol       Date:  2015-04-01

8.  Clinical manifestations of IgA nephropathy combined with thin glomerular basement membrane nephropathy in children.

Authors:  Young Ju Hwang; Dong Sub Kim; Cheol Woo Ko; Min Hyun Cho; Tae In Park
Journal:  Kidney Res Clin Pract       Date:  2013-09-04

9.  Thin basement membrane nephropathy: is there genetic predisposition to more severe disease?

Authors:  Constantinos Deltas
Journal:  Pediatr Nephrol       Date:  2008-11-19       Impact factor: 3.714

10.  Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series.

Authors:  Petar Šenjug; Tamara Nikuševa Martić; Marija Šenjug Perica; Maja Oroz; Matija Horaček; Kristina Gotovac Jerčić; Krešimir Galešić; Danica Galešić Ljubanović
Journal:  Croat Med J       Date:  2021-06-30       Impact factor: 1.351

  10 in total

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