Congenital anal atresia is usually treated, most of them can carry on normal life, so it needs to be treated as soon as possible to avoid serious consequences. Congenital anal atresia is a congenital disease, is due to abnormal development of the primitive anus led to the formation of no anal canal, rectum and the outside world can not be accessed, food into the digestive tract can not be discharged through the anus. The diagnosis is very simple: if there is no anus in sight, and there is bloating and vomiting after eating, the diagnosis can be confirmed with imaging tests. Treatment needs to be given as soon as possible. In the case of low anal atresia, it is sufficient to artificially create an anal opening, and normal life can usually be resumed after the operation. If it is a high anal atresia, it is necessary to connect the rectum and the artificial anus, after timely and effective treatment, usually can achieve normal life. However, surgery for high anal atresia is more troublesome, and high anal atresia is often accompanied by other deformities, the prognosis is relatively poor, so it is necessary to follow the doctor’s instructions in time for treatment. If you are diagnosed with congenital anal atresia, it is recommended that you undergo standardized treatment as soon as possible in order to reduce the adverse effects of the disease.