Congenital Urogenital Malformations
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Transcript Congenital Urogenital Malformations
Prefinal
Topics
Renal agenesis
Renal hypoplasia
Renal fusion
Ectopic kidney
Ureteral atresia
Duplication of the
ureter
Supernumerary
kidneys
Renal agenesis
Virtually always unilateral.
Kidney is either absent or
undeveloped.
Usually causes no symptoms and
found incidentally.
Renal Agenesis
Renal hypoplasia
May appear as one small kidney with
the other one larger than normal.
Small kidneys also have small arteries
and are associated with hypertension
requiring nephrectomy.
Renal hypoplasia
Renal fusion (horseshoe
kidney)
Prevalence 1 in 1,000 people.
Most frequent abnormality seen is a
horseshoe kidney containing 2
excretory systems and 2 ureters.
Usually asymptomatic but are prone to
obstruction.
Renal fusion (horseshoe
kidney)
Ectopic (Pelvis Kidney)
In simple ectopy, the kidney does not
ascend properly and is found in the
pelvis or over the brim.
Prone to obstruction and infection.
Less commonly crossed ectopy without
fusion. The kidney then lies on the
opposite side and is not attached to the
normally placed kidney.
Ectopic Kidney (Pelvis
Kidney)
Ureteral atresia
The ureter may be absent or fails to extend to
the bladder and therefore with a blind
ending.
It is associated with ipsilateral absent or
multicystic kidney.
Bilateral atresia is incompatible with life.
Unilateral atresia is usually asymptomatic
but may cause hypertension.
Ureteral atresia
Duplication of the ureter
One of the most common congenital
malformations of the urinary tract with
duplication found in 0.9% of a series of
autopsies.
More common in females and is often
bilateral.
Often asymptomatic but commonly presents
with persistent or recurrent urinary tract
infections.
Duplication of the ureter
Supernumerary kidneys
Third kidney is very rare and not to be
confused with the relatively common
unilateral duplication of the renal
pelvis.
Supernumerary kidneys