Literature DB >> 12811648

Urinary tract infections, VUR, and autosomal dominant polycystic kidney disease.

Oren Koslowe1, Rachel Frank, Bernard Gauthier, Marcela Vergara, Howard Trachtman.   

Abstract

This case series of 16 patients with autosomal dominant polycystic kidney disease (ADPKD) describes 4 girls who presented with a urinary tract infection (UTI). Radiological evaluation revealed that each of these patients had vesicoureteral reflux (VUR). The frequency of VUR was significantly higher in the patients with ADPKD compared with otherwise healthy age-matched children who underwent testing after a UTI (100% versus 15%, P<0.002). These findings suggest VUR is an associated somatic anomaly in children with ADPKD that may contribute to the occurrence of UTI in this patient population.

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Year:  2003        PMID: 12811648     DOI: 10.1007/s00467-003-1211-4

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


  8 in total

Review 1.  Vesicoureteral reflux.

Authors:  R M Decter
Journal:  Pediatr Rev       Date:  2001-06

Review 2.  Polycystin: new aspects of structure, function, and regulation.

Authors:  Patricia D Wilson
Journal:  J Am Soc Nephrol       Date:  2001-04       Impact factor: 10.121

3.  Interaction of the leucine-rich repeats of polycystin-1 with extracellular matrix proteins: possible role in cell proliferation.

Authors:  Ashraf N Malhas; Ramadan A Abuknesha; Robert G Price
Journal:  J Am Soc Nephrol       Date:  2002-01       Impact factor: 10.121

4.  Utility of ultrasonography in the diagnosis of autosomal dominant polycystic kidney disease in children.

Authors:  P A Gabow; W J Kimberling; J D Strain; M L Manco-Johnson; A M Johnson
Journal:  J Am Soc Nephrol       Date:  1997-01       Impact factor: 10.121

5.  Progression of autosomal-dominant polycystic kidney disease in children.

Authors:  G M Fick-Brosnahan; Z V Tran; A M Johnson; J D Strain; P A Gabow
Journal:  Kidney Int       Date:  2001-05       Impact factor: 10.612

6.  Vascular expression of polycystin.

Authors:  M D Griffin; V E Torres; J P Grande; R Kumar
Journal:  J Am Soc Nephrol       Date:  1997-04       Impact factor: 10.121

7.  Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen.

Authors:  K Zerres; G Mücher; L Bachner; G Deschennes; T Eggermann; H Kääriäinen; M Knapp; T Lennert; J Misselwitz; K E von Mühlendahl
Journal:  Nat Genet       Date:  1994-07       Impact factor: 38.330

8.  Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1.

Authors:  D Ravine; R N Gibson; R G Walker; L J Sheffield; P Kincaid-Smith; D M Danks
Journal:  Lancet       Date:  1994-04-02       Impact factor: 79.321

  8 in total
  3 in total

1.  A girl with a mutation of the ciliary gene CC2D2A presenting with FSGS and nephronophthisis.

Authors:  Midori Awazu; Mamiko Yamada; Nariaki Asada; Akinori Hashiguchi; Kenjiro Kosaki; Kazuya Matsumura
Journal:  CEN Case Rep       Date:  2021-08-25

2.  Chronic asymptomatic pyuria precedes overt urinary tract infection and deterioration of renal function in autosomal dominant polycystic kidney disease.

Authors:  Jin Ho Hwang; Hayne Cho Park; Jong Cheol Jeong; Seon Ha Baek; Mi Yeun Han; Kitae Bang; Jeong Yeon Cho; Suk Hee Yu; Jaeseok Yang; Kook-Hwan Oh; Young-Hwan Hwang; Curie Ahn
Journal:  BMC Nephrol       Date:  2013-01-07       Impact factor: 2.388

3.  Vesicourethral reflux in pediatrics with hypermobility syndrome.

Authors:  Fatemeh Beiraghdar; Zohreh Rostami; Yunes Panahi; Behzad Einollahi; Mojtaba Teimoori
Journal:  Nephrourol Mon       Date:  2013-08-12
  3 in total

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