Ces Urol 2001, 5(2):41-43 | DOI: 10.48095/cccu2001020
Authors present a case report of a boy with incomplete urethral duplicity of epispadic type, associated with bilateral defect of testicular descend and esophageal atresia. Cryptorchidism and esophageal anomaly have required an operative correction, the urethral duplication does nor require any treatment. The described combination of multiple congenital anomalies is rare.
Published: March 1, 2001