| Literature DB >> 8975556 |
J Antón-Pacheco1, J C Ruiz de la Roja, E Martín Oses, E Sánchez Sánchez, M Luján Galán.
Abstract
Urethral duplication is a very rare malformation which occurs almost exclusively in males. Associated genital and urinary malformations are frequent, and the approach in symptomatic cases in surgical management. This paper presents one case of a full double urethra in a 9-year old girl with repeat urinary infections and incontinence. The accessory urethra was surgically removed using perianal and abdominal access. Evolution has been favourable with disappearance of symptomatology.Entities:
Mesh:
Year: 1996 PMID: 8975556
Source DB: PubMed Journal: Actas Urol Esp ISSN: 0210-4806 Impact factor: 0.994