This report describes a rare case of type IIA2 sagittal urethral duplication. The presentation, investigation, and management of this rare anomaly are briefly discussed. A 3½-year-old boy presented with urinary obstruction and recurrent urinary tract infection due to a stenosed dorsal urethra and segmental stenosis of the dominant ventral urethra. The child also had left-sided vesicoureteric reflux. Staged surgical management consisted of an initial vesicostomy followed by serial dilatation of the ventral urethral stricture, left ureteric reimplantation, and a 2-cm long distal urethrourethrostomy between the dorsal urethra, opening at the tip of the penis, and the ventral urethra, which had a hypospadic opening at the base of the glans. The...
Urethral duplication is rare and procedures of management should be individualized according to each...
Urethral duplication is a rare congenital anomaly of the lower urinary system and has varied present...
There are numerous types of urethral duplication previously described in the literature including a ...
Objective This report describes a rare case of type IIA2 sagittal urethral duplication. Summary ba...
Urethral duplication is a rare congenital anomaly, usually found with multiple anatomical variants. ...
Urethral duplication is a rare congenital anomaly, with multiple described anatomical variants. Dupl...
Urethral duplication is a rare congenital anomaly. We report a 6-year-old male with type IIA2 (Y-typ...
To evaluate the medium-term outcomes of the management of children with urethral duplication. We re...
Purpose: To present our experience in urethral duplication focusing on detailed surgical management....
Urethral duplication is a rare congenital anomaly. In addition to a normally urethra, there is an ac...
ABSTRACT Introduction and objective Urethral duplication is a rare congenital anomaly, with roughly...
Copyright © 2014 Kenichi Mori et al. This is an open access article distributed under the Creative C...
Duplication of urethra is a rare congenital anomaly; a Y-shaped urethral duplication is the rarest v...
A non-typical variant of Y-type urethral duplication has been described in the article. In this case...
AbstractThere are numerous types of urethral duplication previously described in the literature incl...
Urethral duplication is rare and procedures of management should be individualized according to each...
Urethral duplication is a rare congenital anomaly of the lower urinary system and has varied present...
There are numerous types of urethral duplication previously described in the literature including a ...
Objective This report describes a rare case of type IIA2 sagittal urethral duplication. Summary ba...
Urethral duplication is a rare congenital anomaly, usually found with multiple anatomical variants. ...
Urethral duplication is a rare congenital anomaly, with multiple described anatomical variants. Dupl...
Urethral duplication is a rare congenital anomaly. We report a 6-year-old male with type IIA2 (Y-typ...
To evaluate the medium-term outcomes of the management of children with urethral duplication. We re...
Purpose: To present our experience in urethral duplication focusing on detailed surgical management....
Urethral duplication is a rare congenital anomaly. In addition to a normally urethra, there is an ac...
ABSTRACT Introduction and objective Urethral duplication is a rare congenital anomaly, with roughly...
Copyright © 2014 Kenichi Mori et al. This is an open access article distributed under the Creative C...
Duplication of urethra is a rare congenital anomaly; a Y-shaped urethral duplication is the rarest v...
A non-typical variant of Y-type urethral duplication has been described in the article. In this case...
AbstractThere are numerous types of urethral duplication previously described in the literature incl...
Urethral duplication is rare and procedures of management should be individualized according to each...
Urethral duplication is a rare congenital anomaly of the lower urinary system and has varied present...
There are numerous types of urethral duplication previously described in the literature including a ...