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School of Medicine >   Department of Urology >   Pediatric Urology >   Hypospadias

Pediatric Urology

Hypospadias

This is a congenital problem present in some newborn boys (occurring approximately in 1:250 male births). This describes an abnormality whereby the opening is not at the very end of the head of the penis. The opening from which the stream emanates may be malpositioned on the bottom of the penis-anywhere from the head of the penis to the scrotal area. There may also be an associated bend or curvature downward, called chordee. The further removed the opening is from the end of the penis, the more likely that a chordee be present. Circumcision should not be done in infants with hypospadias, since the foreskin is often used in the requisite corrective surgery.

Surgical correction is best accomplished between six months to one year of age via ambulatory surgery under general anesthesia. As noted above, the foreskin may be used for creation of the new urinary channel and/or coverage of the bottom surface of the penis when chordee is present. Post procedure, one can anticipate both an excellent cosmetic and functional result.



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Last Modified on 04/30/2008