What happens when a child is born with a crooked urethra?

Children with crooked urethral opening, medically known as hypospadias, is a common congenital malformation of the urinary system, and early treatment is advisable.
Hypospadias is caused by the longitudinal urogenital septum on the ventral side of the genital node from back to front growth closure process stops, often have the following characteristics: urethral opening of the abnormality, dorsal side of the penis foreskin is normal and the penis ventral side of the foreskin missing, the penis to the ventral side of the curved, urethral spongy underdevelopment and so on.
Some types of hypospadias can affect sexual function and sexual behavior, requiring sitting to urinate in life, and can also bring about psychological disorders due to deformed genitals. Reconstructive surgery is recommended to restore normal standing urination as well as normal sexual activity in adulthood. Surgery should be performed before school age and can be done in one or more stages.
In summary, if any of the above symptoms are present, it is important to seek medical attention.