Congenital anomalies of the lower urinary tract (CALUT) are a family of birth defects of the
ureter, the bladder, and the urethra. CALUT includes ureteral anomaliesc such as congenital …

Routine prenatal sonography has made prenatal anomaly detection a reality. Congenital
anomalies affect up to 2% of all pregnancies, 1, 2 and ultrasound technology has high …

Objectives The purpose of this study was to evaluate the prenatal findings and postnatal
outcomes in fetuses with congenital megalourethra. Methods This retrospective study …

Summary Introduction Congenital Lower Urinary Tract Obstructions (LUTO) is a
heterogeneous group of diseases in which urine elimination is obstructed at the level of …

Background Congenital megalourethra is a urogenital anomaly characterized by a cystic
dilatation and elongation of the penile urethra resulting from the absence and hypoplasia of …

Background. Congenital megalourethra is an uncommon cause of lower urinary tract
obstruction that is rarely prenatally diagnosed in second trimester sonographic examination …

Congenital anterior urethrocutaneous fistula and megalourethra are both rare anomalies.
These anomalies are commonly associated with other anorectal or genitourinary anomalies …

Background To describe the perinatal outcomes of fetoscopic urethral meatotomy (FUM) in
fetuses with lower urinary tract obstruction (LUTO) by congenital megalourethra. Study …

Fetal lower urinary tract obstruction [LUTO] represents a rare, heterogeneous group of
uropathies involving mechanical or functional blockage at the bladder outlet of varying …

Cysts are uncommon congenital lesions of the fetal penis. Fetal penile cysts can develop
when epithelial cells become entrapped during the fusion of the labial scrotal folds. The …