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Erschienen in: Pediatric Nephrology 7/2008

01.07.2008 | Review

Gene discovery and vesicoureteric reflux

verfasst von: Inga J. Murawski, Indra R. Gupta

Erschienen in: Pediatric Nephrology | Ausgabe 7/2008

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Abstract

Vesicoureteric reflux (VUR) is a congenital urinary tract defect caused by abnormal insertion of the ureter within the bladder wall. This leads to a defective ureterovesical junction in which urine flows retrogradely from the bladder to the kidneys. Although VUR is associated with recurrent urinary tract infections, renal malformations, hypertension, and reflux nephropathy, its relationship to each of these clinical entities is poorly understood. Mutations in genes expressed by the developing kidney and urinary tract can cause VUR in mice, and some of these same genes have been identified in humans with VUR. By discovering the genes that are associated with VUR, new hypotheses will be generated such that, eventually, the relationship between VUR and its complications will be understood.
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Zurück zum Zitat Kelly H, Molony CM, Darlow JM, Pirker ME, Yoneda A, Green AJ, Puri P, Barton DE (2007) A genome-wide scan for genes involved in primary vesicoureteric reflux. J Med Genet 44(11):710–717PubMedPubMedCentralCrossRef Kelly H, Molony CM, Darlow JM, Pirker ME, Yoneda A, Green AJ, Puri P, Barton DE (2007) A genome-wide scan for genes involved in primary vesicoureteric reflux. J Med Genet 44(11):710–717PubMedPubMedCentralCrossRef
Metadaten
Titel
Gene discovery and vesicoureteric reflux
verfasst von
Inga J. Murawski
Indra R. Gupta
Publikationsdatum
01.07.2008
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Nephrology / Ausgabe 7/2008
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-007-0704-y

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