Literature DB >> 6668201

Renal disorders in the branchio-oto-renal syndrome.

J Widdershoven, L Monnens, K Assmann, C Cremers.   

Abstract

Intravenous urography and measurements of renal function were performed in 16 patients suffering from branchio-oto-renal syndrome. Malformations were visible by intravenous urography in all patients. Four out of 16 patients had a diminished glomerular filtration rate. Renal histology available in two patients revealed oligomeganephronic renal hypoplasia and multicystic dysplasia, respectively. Without renal agenesis or severe renal hypoplasia or dysplasia present in early infancy, renal abnormality does not seem to be a progressive disorder.

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Year:  1983        PMID: 6668201

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN: 0018-022X


  3 in total

1.  Is unilateral multicystic renal dysplasia sometimes heritable, and what is the risk of recurrence?

Authors:  J Bernstein
Journal:  Pediatr Nephrol       Date:  1990-11       Impact factor: 3.714

2.  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

3.  EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions.

Authors:  Michiyo Okada; Rika Fujimaru; Noriko Morimoto; Kenichi Satomura; Yoshikazu Kaku; Kazuo Tsuzuki; Kandai Nozu; Torayuki Okuyama; Kazumoto Iijima
Journal:  Pediatr Nephrol       Date:  2006-02-21       Impact factor: 3.714

  3 in total

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