Infantile hypospadias is a congenital disease. Its clinical symptoms: first, the urethral opening position is abnormal, under normal circumstances, the urethral opening in the middle of the penis head, but the urethral hypospadias children can be seen in the middle of the depression, and the urethral opening is located in the coronal groove of the penis, the body of the penis, or the root of the urethral opening, serious children, the opening of the perineum can not be stood in the region of the urinary bladder. Second, downward curvature of the penis deformity, hypospadias children due to urethral fusion disorder, the urethral opening of the distal spongy body adjacent to the deep fascia, sarcolemma development is incomplete, can cause the penis downward curvature, can not be normal erection, affecting sexual intercourse. Third, the foreskin distribution is abnormal, the affected children mostly appear to be missing foreskin at the tie, while the dorsal foreskin is piled up, forming a turban-like or hat-like superposition. Fourth, children with severe hypospadias may also be accompanied by scrotal splitting, penoscrotal malposition, etc., and even the possibility of being considered a baby girl at the early stage of birth.