نتایج جستجو برای: vesicoureteric reflux

تعداد نتایج: 18224  

2009
O. J. Arthurs I. Joubert M. J. Graves D. J. Lomas

Introduction Vesico-ureteric reflux (VUR) is a congenital disorder of the paediatric renal tract, which allows the retrograde passage of urine up to the renal pelvis, predisposing to renal infection and consequential scarring, hypertension and renal failure. The current gold standard for diagnosis is the Micturating Cystourethrogram (MCUG), allowing snap-shot imaging of the urethra, bladder and...

Journal: :Journal of Society of Surgeons of Nepal 2022

Introduction: Cohen’s cross trigonal ureteric reimplantation is the gold standard for surgical management of vesicoureteric reflux (VUR) in children with high success rate. The objective this study was to evaluate and assess outcome open procedure VUR.
 Methods: A retrospective review all patients VUR who underwent between March 2010 February 2020 done. following were recorded each patient...

Journal: :Archivos espanoles de urologia 2008
Delphine Demède Pierre Mouriquand

Vesicoureteral reflux remains one of the most controversial subjects in paediatric urology. The flooding of publications on reflux makes the understanding of this anomaly and its treatments quite opaque. Evidence Based Medicine might be a helpful tool to clarify the various approaches of reflux reflected in 6.715 publications found on Medline with the key-words "vesicoureteral reflux" and "vesi...

2013
Shweta Prasad Amrit Kaur Kaler Shameem Shariff

Ask-Upmark Kidney or Renal segmental hypoplasia is a rare congenital kidney disorder associated with hypertension. It was first described by Eric Ask-Upmark in 1929 as congenital unilateral renal hypoplasia. This is a report of 2 cases detected over a 5 year period. The first case is of an 11 month old female who presented with repeated haematuria. Investigations revealed a small, non-functioni...

Journal: :Human molecular genetics 1996
M R Eccles R R Bailey G D Abbott M J Sullivan

Primary vesicoureteric reflux (VUR) is one of the more common genetic disorders. Little is yet known about the genetics of this potentially manageable childhood condition, which is characterised by regurgitation of urine from the bladder to the kidney. The VUR phenotype is associated with shortness of the submucosal segment of the ureter due to congenital lateral ectopia of the ureteric orifice...

Journal: :Archives of disease in childhood 1993
W G Bourke T A Clarke T G Mathews D O'Halpin V B Donoghue

To determine the incidence of silent renal anomalies in infants with isolated single umbilical artery (SUA), all infants with SUA and without other obvious congenital anomalies, identified over a six year period, were screened using renal ultrasonography. Over 35,000 placentas were examined. An isolated single umbilical artery was identified in 112 (0.32%). Nineteen infants had abnormal renal i...

Journal: :Archives of disease in childhood 1996
J M Tibballs R De Bruyn

The presence or absence of pelvicalyceal dilatation on postnatal ultrasound continues to appear within diagnostic algorithms to select patients for micturating cystourethrography (MCU) in the investigation of antenatally diagnosed hydronephrosis. Postnatal ultrasound findings were assessed in a population diagnosed as having antenatal hydronephrosis due solely to primary vesicoureteric reflux (...

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