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Duplicated ureter is a congenital condition in which the ureteric bud, the embryological origin of the ureter, splits resulting in two ureters draining a single kidney (figure 1). It is the most common renal abnormality, occurring in approximately 1% of the population.1 ,2 Duplicated ureter is more common in women. Ureteral duplication is either partial, that is, the two ureters drain into the bladder via a single common ureter or complete in which two ureters drain separately. It can be associated with a variety of congenital genitourinary abnormalities. They are usually asymptomatic and detected incidentally on imaging studies. Excretory urographic findings are almost always diagnostic. Double ureter and duplex system have potential for future complications, such as the collecting system obstruction, lithiasis, ureterocele and vesicoureteral reflux.3 The early detection of the anomalies are helpful in avoiding complications related to the duplex collecting system.
Developmental anomalies of the kidney, ureter and urinary bladder can lead to complications which are preventable.
Early detection of the anomalies can avoid complications related to the duplex collecting system.
Dr Abdul Hai, Assistant Professor, HIMSR, Jamia Hamdard, New Delhi.
Contributors MH was responsible for the conception, design, drafting of the article. FH was responsible for the acquisition of data. AB helped in revising and drafting the article.
Competing interests None.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
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