Abstract
Megalourethra is a rare congenital anomaly characterised by a failure of development of erectile tissue and subsequent dilatation of the penile urethra. The term was first used by Nesbitt (1955) and since then many of these defects concerning the corpus spongiosum and the corpora cavernosa have been reported (Mortensen et al., 1985; Appel et al., 1986; Aigen et al., 1987).Concomitant malformations, which are sometimes incompatible with survival, have important implications for therapy and prognosis. Associated anomalies may involve the urinary tract (renal hypoplasia, ureterohydronephrosis, megaureter, megacystis, reflux, bladder diverticula, hypospadias, manifestations of intersex, urethral valves, prune belly syndrome) as well as other organs (teeth, heart, intestines).
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
