Literature DB >> 12686848

Familial vesicoureteral reflux.

Boris Chertin1, Prem Puri.   

Abstract

PURPOSE: Vesicoureteral reflux is known to occur in families. We summarized worldwide data on the incidence and nature of vesicoureteral reflux in siblings of children with vesicoureteral reflux.
MATERIALS AND METHODS: We searched MEDLINE using the words siblings vesicoureteral reflux, familial vesicoureteral reflux, offspring vesicoureteral reflux and vesicoureteral reflux screening. All articles that we identified that were published from 1972 to 2002 were analyzed for the incidence of renal damage in siblings of patients with vesicoureteral reflux.
RESULTS: Siblings of patients with vesicoureteral reflux have a much higher incidence of reflux than the normal population. There is a direct relationship of patient age to the incidence and severity of reflux. Most investigators advocate screening asymptomatic siblings of patients with vesicoureteral reflux.
CONCLUSIONS: The incidence of sibling reflux is significant. When vesicoureteral reflux is discovered in symptomatic siblings, it is usually high grade and associated with a high incidence of reflux nephropathy. Randomized controlled studies are needed to compare renal damage in patients with reflux detected through screening to renal damage in those diagnosed after urinary tract infection to establish how much renal damage may be prevented by screening in asymptomatic siblings.

Entities:  

Mesh:

Year:  2003        PMID: 12686848     DOI: 10.1097/01.ju.0000058428.00284.d5

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  12 in total

1.  A genome-wide scan for genes involved in primary vesicoureteric reflux.

Authors:  H Kelly; C M Molony; J M Darlow; M E Pirker; A Yoneda; A J Green; P Puri; D E Barton
Journal:  J Med Genet       Date:  2007-07-27       Impact factor: 6.318

Review 2.  Urinary tract infection in children: recurrent infections.

Authors:  James Larcombe
Journal:  BMJ Clin Evid       Date:  2015-06-12

Review 3.  Urinary tract infection in children.

Authors:  James Larcombe
Journal:  BMJ Clin Evid       Date:  2010-02-09

4.  Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation.

Authors:  Bradley W McDill; Song-Zhe Li; Paul A Kovach; Li Ding; Feng Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-25       Impact factor: 11.205

Review 5.  Applying the ALARA concept to the evaluation of vesicoureteric reflux.

Authors:  Richard S Lee; David A Diamond; Jeanne S Chow
Journal:  Pediatr Radiol       Date:  2006-09

6.  A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5.

Authors:  Christine E Briggs; Chao-Yu Guo; Cynthia Schoettler; Ilina Rosoklija; Andres Silva; Stuart B Bauer; Alan B Retik; Louis Kunkel; Hiep T Nguyen
Journal:  Eur J Hum Genet       Date:  2009-08-19       Impact factor: 4.246

7.  Primary Vesico-Ureteral Reflux: Comparison of Factors between Infants and Children.

Authors:  Hyeon Chan Jang; Kyung Hun Lee; Jae Shin Park
Journal:  Korean J Urol       Date:  2011-03-18

8.  The current evidence based medical management of vesicoureteral reflux: The Sickkids protocol.

Authors:  Sumit Dave; Antoine E Khoury
Journal:  Indian J Urol       Date:  2007-10

9.  A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity.

Authors:  Maria Luisa Conte; Aida M Bertoli-Avella; Bianca M de Graaf; Francesca Punzo; Giuliana Lama; Angela La Manna; Carolina Grassia; Pier Francesco Rambaldi; Ben A Oostra; Silverio Perrotta
Journal:  Pediatr Nephrol       Date:  2008-01-16       Impact factor: 3.714

10.  A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development.

Authors:  J M Darlow; M G Dobson; R Darlay; C M Molony; M Hunziker; A J Green; H J Cordell; P Puri; D E Barton
Journal:  Mol Genet Genomic Med       Date:  2013-07-07       Impact factor: 2.183

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