Posterior urethral stenosis in newborn with renal nonfunction syndrome

A newborn male infant presented with the “renal nonfunction syndrome” and subsequently was found at autopsy to have congenital stenosis of the posterior urethra. Additional urinary tract malformations included a prostatic diverticulum, bladder hypertrophy, bilateral hydroureter, and bilateral renal...

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Veröffentlicht in:Urology (Ridgewood, N.J.) N.J.), 1978-06, Vol.11 (6), p.624-628
Hauptverfasser: Lehmiller, David J., Kanto, William P.
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creator Lehmiller, David J.
Kanto, William P.
description A newborn male infant presented with the “renal nonfunction syndrome” and subsequently was found at autopsy to have congenital stenosis of the posterior urethra. Additional urinary tract malformations included a prostatic diverticulum, bladder hypertrophy, bilateral hydroureter, and bilateral renal hypoplasia with dysplasia. Autopsy evidence suggested that the urethral stenosis had manifested itself very early during embryologic development and accounted for the associated urinary anomalies. The infant had the physical stigmata, clinical course, and pulmonary hypoplasia commonly observed in “Potter’s” or the “renal nonfunction syndrome.”
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Abnormalities, Multiple
Humans
Infant, Newborn
Kidney Diseases - congenital
Male
Syndrome
Urethral Stricture - congenital
Urethral Stricture - embryology
Urethral Stricture - pathology
Urinary Tract - abnormalities
Urinary Tract - pathology
title Posterior urethral stenosis in newborn with renal nonfunction syndrome
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