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Prog Urol ; 20(3): 233-7, 2010 Mar.
Article in French | MEDLINE | ID: mdl-20230948

ABSTRACT

A stenosis of the upper pole of an incomplete renal duplication is presented. The prenatal diagnosis of a right renal ureteropyelic junction syndrome, isolated, with a normal amniotic liquid was confirmed at birth. Intravenous pyelogram 8 days after birth showed three right dilated calical groups with a dilated renal ureteropyelic junction, but an normal inferior calical group suspected a renal bifidity. Renal MagIII scintigraphy evaluated the anatomical and functional stenosis and indicated surgery. Postoperative followings were simple and results good 3 years after. From this rare case, embryogenesis is discussed.


Subject(s)
Abnormalities, Multiple , Kidney Pelvis/abnormalities , Ureter/abnormalities , Abnormalities, Multiple/embryology , Constriction, Pathologic , Humans , Infant, Newborn , Kidney Pelvis/embryology , Male , Ureter/embryology
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