What is anorectal malformation?

anorectal malformation is anomaly in the formation and/or rectum and rectum position, the output for the digestive tract. This congenital defect is relatively rare and occurs in approximately one of every 5,000 births and tends to be more common in men. Treatment includes surgery to repair malformation and in some cases multiple surgical procedures may be necessary to solve the problem. The condition is usually identified shortly after birth because it tends to be visually obvious. In some cases, there seems to be a genetic component. The anorectal malformation is associated with several genetic diseases and there is an increased risk of its origin in families with a history of this condition. In other cases, it seems random in nature and there are no identifiable risk factors.

In the child with anorektal malformations, the anus will be forward before expected. Sometimes the intestine enters the genitourine tract. Children may also have imprient anus where there is no sales on the outsideOJ is a condition requiring immediate operation to create a feces for feces before developing complications due to the inability to defecate. Treatment includes plastic surgery to relocate the rectum and rectum and, in the case of an imperfire rectum, to create a new rectum so that the child can express the feces.

The complexity of surgery varies depending on the nature of the case. Sometimes the child must be equipped with colostomy and a number of operations are performed to move the rectum and rectum, problems with the repair and rebuilding of the rectum. In other cases, surgery is relatively simple and only one procedure is needed to relocate the rectum and correction of anorectal malformation.

Sometimes, the pineapple malformation is gentle and may not be recorded immediately after birth. In these cases, problems may develop on days immediately after birth. Pediatricians can evaluate infants with themThey seem to have problems with their intestinal tract to look for signs of congenital anomalies that could be responsible for the problem, and if surgery occur, they can refer their patients to the surgeon. In general, people with this condition do not need support for subsequent monitoring as soon as their operations are complete and normally defined. If the condition is accompanied by other abnormalities of the digestive tract, the patient may need special food or other measures.