Literature DB >> 7107121

Glomerular lesions in the branchio-oto-renal (BOR) syndrome.

R Dumas, A Uziel, P Baldet, A Segond.   

Abstract

Three cases: two adults and one child, with histologically confirmed branchio-oto-renal syndrome showed prominent glomerular lesions. Typically there was segmental and focal hyalinization associated with dense deposits along the basement membrane and in the mesangium. Variable deposits of immunoglobulins IgG, IgM, and IgA as well as C3 were present. The branchio-oto-renal syndrome appears to be a familial nephropathy which may lead to renal failure.

Entities:  

Mesh:

Year:  1982        PMID: 7107121

Source DB:  PubMed          Journal:  Int J Pediatr Nephrol        ISSN: 0391-6510


  2 in total

1.  Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree.

Authors:  R König; S Fuchs; C Dukiet
Journal:  Eur J Pediatr       Date:  1994-06       Impact factor: 3.183

2.  A Perihilar Variant of Focal Segmental Glomerulosclerosis Due to De novo Branchio-oto-renal Syndrome.

Authors:  Ryosuke Saiki; Kan Katayama; Masako Kitano; Kayo Tsujimoto; Fumika Tanaka; Yasuo Suzuki; Tomohiro Murata; Tairo Kurita; Ryuji Okamoto; Kazuhiko Takeuchi; Kaoru Dohi
Journal:  Intern Med       Date:  2021-12-04       Impact factor: 1.282

  2 in total

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