Literature DB >> 17849152

End-stage renal failure, reflux nephropathy and Feingold's syndrome.

Mona Aslam1, Hans van Bokhoven, Christopher Mark Taylor.   

Abstract

Feingold's syndrome is a recognised syndrome of organ maldevelopment. Renal abnormalities are not a consistent feature. We report the case of a girl with Feingold's syndrome who had developed end-stage renal failure by the age of 6 years. We recommend that urinary tract imaging be carried out in all children suspected of having Feingold's syndrome.

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Year:  2007        PMID： 17849152     DOI： 10.1007/s00467-007-0602-3

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


  10 in total

1.  Loss of N-myc function results in embryonic lethality and failure of the epithelial component of the embryo to develop.

Authors:  B R Stanton; A S Perkins; L Tessarollo; D A Sassoon; L F Parada
Journal:  Genes Dev       Date:  1992-12       Impact factor: 11.361

2.  Vertebral anomalies in a new family with ODED syndrome.

Authors:  L D Piersall; S B Dowton; W H McAlister; D J Waggoner
Journal:  Clin Genet       Date:  2000-06       Impact factor: 4.438

3.  N-myc is essential during neurogenesis for the rapid expansion of progenitor cell populations and the inhibition of neuronal differentiation.

Authors:  Paul S Knoepfler; Pei Feng Cheng; Robert N Eisenman
Journal:  Genes Dev       Date:  2002-10-15       Impact factor: 11.361

4.  Familial syndromic esophageal atresia maps to 2p23-p24.

Authors:  J Celli; E van Beusekom; R C Hennekam; M E Gallardo; D F Smeets; S R de Córdoba; J W Innis; M Frydman; R König; H Kingston; J Tolmie; L C Govaerts; H van Bokhoven; H G Brunner
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

5.  MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

Authors:  Hans van Bokhoven; Jacopo Celli; Jeroen van Reeuwijk; Tuula Rinne; Bob Glaudemans; Ellen van Beusekom; Paul Rieu; Ruth A Newbury-Ecob; Chin Chiang; Han G Brunner
Journal:  Nat Genet       Date:  2005-04-10       Impact factor: 38.330

6.  Imperforate anus in Feingold syndrome.

Authors:  V Büttiker; J Wojtulewicz; M Wilson
Journal:  Am J Med Genet       Date:  2000-05-29

7.  MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome.

Authors:  M Frydman; M Katz; S G Cabot; G Soen; A Kauschansky; L Sirota
Journal:  Am J Med Genet       Date:  1997-08-22

Review 8.  Feingold syndrome: clinical review and genetic mapping.

Authors:  Jacopo Celli; Hans van Bokhoven; Han G Brunner
Journal:  Am J Med Genet A       Date:  2003-11-01       Impact factor: 2.802

9.  Embryonic lethality resulting from disruption of both N-myc alleles in mouse zygotes.

Authors:  S Sawai; A Shimono; K Hanaoka; H Kondoh
Journal:  New Biol       Date:  1991-09

10.  Embryonic lethality in mice homozygous for a targeted disruption of the N-myc gene.

Authors:  J Charron; B A Malynn; P Fisher; V Stewart; L Jeannotte; S P Goff; E J Robertson; F W Alt
Journal:  Genes Dev       Date:  1992-12       Impact factor: 11.361
  10 in total
  1 in total

Review 1.  MicroRNAs: potential regulators of renal development genes that contribute to CAKUT.

Authors:  April K Marrone; Jacqueline Ho
Journal:  Pediatr Nephrol       Date:  2013-09-03       Impact factor: 3.714
  1 in total

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