Interrupted descent of testis leads to an empty scrotal sac and abnormal location of the testis, which can lie anywhere along the usual route of descent. Most commonly the testis is present in the inguinal canal, where it can be palpated. This condition is usually diagnosed at birth or within the first year of life. A higher incidence of ectopic (undescended) testis occurs in premature births (30%) than in term births (3–5%). Normally, the ectopic testis can complete its descent within the first 3 months after a child is born; therefore watchful waiting is recommended for the first couple of months. A specialist referral is usually made at 6 months if the testis is still absent from the scrotal sac. It is crucial to make the diagnosis early so that an appropriate management plan can be initiated to avoid or reduce the risk of complications such as testicular malignancy, subfertility or infertility, testicular torsion, and inguinal hernia (due to patent processus vaginalis). If surgical correction is required, the ectopic testis is moved from the inguinal canal into the scrotum (orchiopexy). During mobilization of the testis, dissection of tissues must be performed carefully to avoid injuring the ilioinguinal nerve adjacent to the spermatic cord. At the time of orchiopexy, the patent processus vaginalis is closed and any inguinal hernia, if present, is repaired.