Literature DB >> 3020315

[Terminal renal failure in aniridia-Wilms syndrome].

H Wilms, E Back, G Kirste.   

Abstract

Missing iris combined with debility and incidence of Wilms' tumor seem to be a complex syndrome which appears in 1:100,000 people. It is caused by an interstitial deletion on the short arm of chromosome no. 11. We refer to a patient who developed end-stage renal failure caused by a focal-segmental nephrosclerosis. He underwent renal transplantation because chronic hemodialysis was impossible due to his lack of compliance. The deletion of chromosome 11 could be recognized by chromosomal analysis after transplantation. An aniridia-Wilms' tumor association (AWTA) with following focal segmental nephrosclerosis could be diagnosed.

Entities:  

Mesh:

Year:  1986        PMID: 3020315     DOI: 10.1007/bf01732191

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  21 in total

1.  [Wilms' nephroblastoma and congenital renal diseases in the case reports of the Istituto Provinciale di Protezione ed Assistenza dell'Infanzia di Milano].

Authors:  P BRUSA; C TORRICELLI
Journal:  Minerva Pediatr       Date:  1953-06-30       Impact factor: 1.312

2.  Aniridia caused by a heritable chromosome 11 deletion.

Authors:  H M Hittner; V M Riccardi; U Francke
Journal:  Ophthalmology       Date:  1979-06       Impact factor: 12.079

3.  Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 17-1985. A 13-year-old boy with aniridia and proteinuria 11 years after nephrectomy for a Wilms' tumor.

Authors: 
Journal:  N Engl J Med       Date:  1985-04-25       Impact factor: 91.245

4.  Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature.

Authors:  C Turleau; J de Grouchy; M F Tournade; M F Gagnadoux; C Junien
Journal:  Clin Genet       Date:  1984-10       Impact factor: 4.438

5.  [Aniridia and Wilms' tumor (Miller's syndrome)].

Authors:  R Rochels
Journal:  Klin Padiatr       Date:  1981-05       Impact factor: 1.349

6.  The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases.

Authors:  R Habib; C Loirat; M C Gubler; P Niaudet; A Bensman; M Levy; M Broyer
Journal:  Clin Nephrol       Date:  1985-12       Impact factor: 0.975

7.  Gene dose effect: intraband mapping of the LDH A locus using cells from four individuals with different interstitial deletions of 11p.

Authors:  U Francke; D L George; M G Brown; V M Riccardi
Journal:  Cytogenet Cell Genet       Date:  1977

8.  Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

Authors:  E R Fearon; B Vogelstein; A P Feinberg
Journal:  Nature       Date:  1984 May 10-16       Impact factor: 49.962

9.  Arterial hypertension developing 10 years after radiotherapy for Wilms's tumour.

Authors:  O Koskimies
Journal:  Br Med J (Clin Res Ed)       Date:  1982-10-09

10.  Hemodynamically mediated glomerular injury and the progressive nature of kidney disease.

Authors:  B M Brenner
Journal:  Kidney Int       Date:  1983-04       Impact factor: 10.612

View more
  1 in total

1.  End stage renal disease in patients with Wilms tumor: results from the National Wilms Tumor Study Group and the United States Renal Data System.

Authors:  Norman E Breslow; Allan J Collins; Michael L Ritchey; Yevgeny A Grigoriev; Susan M Peterson; Daniel M Green
Journal:  J Urol       Date:  2005-11       Impact factor: 7.450

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.