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Ectopic ureters are found in 1 of every 2000–4000 patients, [6] and can be difficult to diagnose, but are most often seen on CT scans. [7] Ectopic ureter is commonly a result of a duplicated renal collecting system, a duplex kidney with 2 ureters. In this case, usually one ureter drains correctly to the bladder, with the duplicated ureter ...
Duplicated ureter is the most common renal abnormality, occurring in approximately 1% of the population. [2] It occurs in about 0.7% of healthy adults and in 2% to 4% of people with urinary tract issues. [4] Race Duplicated ureter is more common in White Americans than in African-Americans. [citation needed] Sex Duplicated ureter is more common ...
A ureterocele is a congenital abnormality found in the ureter. In this condition the distal ureter balloons at its opening into the bladder, forming a sac-like pouch. It is most often associated with a duplicated collection system, where two ureters drain their respective kidney instead of one. Simple ureterocele, where the condition involves ...
In children, hydronephrosis can be caused by ureteropelvic junction obstruction, ectopic inserted ureter, primary megaureter and posterior urethral valve (Figure 13). In the latter, both kidneys will be affected. In adults, hydronephrosis can be caused by urolithiasis, obstructing the outlet of the renal pelvis or the ureter, and compression of ...
The ureters can be affected by a number of diseases, including urinary tract infections and kidney stone. Stenosis is when a ureter is narrowed, due to for example chronic inflammation. Congenital abnormalities that affect the ureters can include the development of two ureters on the same side or abnormally placed ureters. Additionally, reflux ...
Ectopic thymus, where thymus tissue is found in an abnormal location; Ectopic thyroid, where an entire or parts of the thyroid are located elsewhere in the body; Ectopic tooth, a tooth that erupted outside the dental arch; Ectopic ureter, where the ureter terminates somewhere other than the urinary bladder
Alport syndrome is a genetic disorder [1] affecting around 1 in 5,000–10,000 children, [2] characterized by glomerulonephritis, end-stage kidney disease, and hearing loss. [3] Alport syndrome can also affect the eyes, though the changes do not usually affect vision, except when changes to the lens occur in later life. Blood in urine is universal.
An intravenous pyelogram is used to look for problems relating to the urinary tract. [5] These may include blockages or narrowing, such as due to kidney stones, cancer (such as renal cell carcinoma or transitional cell carcinoma), enlarged prostate glands, and anatomical variations, [5] such as a medullary sponge kidney. [6]