Pediatric imperforate anus

Imperforate anus is a defect that is present from birth congenital. The opening to the anus is missing or blocked. The anus is the opening to the rectum through which stools leave the body. It is caused by abnormal development of the fetus. Many forms of imperforate anus occur with other birth defects. A health care provider can diagnose this condition during a physical exam.
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Imperforate Anus

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Imperforate anus: MedlinePlus Medical Encyclopedia

Imperforate anus is a birth defect that affects about one of every 5, newborns, and is somewhat more common among boys than girls. It may occur alone or together with other abnormalities of the rectum the end of intestine that connects with the anus and anus the body's opening to dispel solid waste. There is no known cause for imperforate anus. If a newborn does not have an anus, there is no outlet to release stool after birth. The intestine ends in a blind pouch, so your infant's stool, called meconium, remains in the intestine. In some cases, the rectum may end high in the pelvis or it can end low, closer to the correct position.
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Imperforate Anus and Anorectal Malformations

Imperforate pronounced im-PURR-for-ate anus means there is no opening for poop stool or feces to leave the body at the end of the digestive tract. This problem can happen in these ways:. Why they happen is not known.
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This is an "umbrella term" for a group of birth defects which affect the anorectal area. During a normal bowel movement, solid waste passes from the colon large intestine to the rectum the final section the colon and through the anus. When a child has an ARM, the rectum and the anus do not develop properly. Some of these problems are very minor and easy to treat, with great long-term prognosis. Others are complex and affect multiple areas of life, such as sexual function and urinary and bowel control.
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