Literature DB >> 10400048

Accuracy of prenatal ultrasonographic diagnosis of duplex renal system.

P Vergani1, P Ceruti, A Locatelli, E Mariani, G Paterlini, C Zorloni, A Ghidini.   

Abstract

Duplex renal system is a rare congenital anomaly of the urinary tract that can be diagnosed in utero. The purpose of this study was to establish the optimal diagnostic criteria for fetal renal duplication in a population undergoing prenatal sonographic screening. Between January 1989 and June 1997 we found 11 cases of duplex renal system, 10 of which were correctly identified in utero at a median gestational age of 28 weeks (range, 20 to 38 weeks), and one of which was a false-negative diagnosis. Prenatal diagnosis of duplex renal system can be made in utero during the second half of pregnancy in the presence of two or more of the following signs: hydronephrosis limited to one pole in a kidney with two separate, noncommunicating renal pelves; ipsilateral megaureter; and ureterocele.

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Year:  1999        PMID: 10400048     DOI: 10.7863/jum.1999.18.7.463

Source DB:  PubMed          Journal:  J Ultrasound Med        ISSN: 0278-4297            Impact factor:   2.153


  2 in total

Review 1.  Postnatal evaluation of infants with an abnormal antenatal renal sonogram.

Authors:  Amy M Becker
Journal:  Curr Opin Pediatr       Date:  2009-04       Impact factor: 2.856

2.  [Retrospective analysis of differential therapeutic measures in children with double kidney and ureter and hydronephrosis].

Authors:  F Eckoldt; K S Heling; B Stöver; R Woderich; S Wolke
Journal:  Urologe A       Date:  2003-03-14       Impact factor: 0.639

  2 in total

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