Duplication of the ureters is a common anomaly and is frequently encou
ntered by radiologists. Duplication may be either complete or incomple
te and is often accompanied by various complications. Incomplete dupli
cation is most often associated with ureteroureteral reflux or uretero
pelvic junction obstruction of the lower pole of the kidney. Complete
duplication is most often associated with vesicoureteral reflux, ectop
ic ureterocele, or ectopic ureteral insertion, all of which are more c
ommon in girls than in boys. Vesicoureteral reflux affects the lower p
ole and can be outgrown,as in nonduplicated systems. Ectopic ureteroce
le and ectopic: ureteral insertion affect the upper pole. The ectopic
ureterocele produces a filling defect of variable size in the bladder;
it can be identified with contrast material studies or ultrasound. Ec
topic ureters may function poorly, be difficult to detect, and cause e
nuresis in girls. A fourth complication, ureteropelvic junction obstru
ction, occurs only in the lower pole and is seen in more boys than gir
ls. Anatomic variants or anomalies as well as suboptimal imaging techn
iques can either simulate or obscure duplication, making diagnosis dif
ficult. However, familiarity with the embryology of duplication and an
awareness of the potential pitfalls of excretory urography and voidin
g cystourethrography will foster an understanding of the varied appear
ances and associated complications of both incomplete and complete dup
lication.