Vesicoureteral reflux (VUR) was recognized neonatally by voiding cysto
graphy in 25 of 117 infants with a dilated fetal urinary tract. There
was a male pre-ponderance (76%) and a high percentage (40%) of associa
ted urinary malformations. Thirtynine refluxing units were studied. Al
l grades of VUR were detected but gross dilating VUR dominated (59%).
Spontaneous resolution was excellent in lower grades of VUR but was po
or in gross VUR. Surgery was successfully performed in 13 renal units
of nine patients with gross reflux [8], additional ipsilateral malform
ations [4], or pyelonephritis during antibiotic prophylaxis [1]. Segme
ntal renal scars developed in four kidneys after urinary infections, a
nd a diffuse parenchymal lesion was noted in nine kidneys even at birt
h. One boy with duplication had a non-functioning refluxing system. Ou
r results in a small number of infants show differences to children wi
th VUR detected after urinary infections and seem to support the exist
ence of a congenital reflux nephropathy.