The anus is either not present or it is in the
wrong place. There are basically two kinds of anal atresia. In boys with high
anal atresia, there may be a channel (fistula) connecting the large intestine
to either the urethra (which delivers urine from the bladder) or the bladder
itself. In girls, the channel may connect with the vagina. Sixty percent of
children with high anal atresia have other defects, including problems with the
esophagus, urinary tract, and bones. In low anal atresia, the channel may open
in front of the circular mass of muscles that constrict to close the anal
opening (anal sphincter) or, in boys, below the scrotum. Occasionally, the
intestine ends just under the skin. It is estimated that overall abnormalities
of the anus and rectum occur in about one in every 5,000 births and are
slightly more common among boys. A mother who has one child with these kind of
conditions has a 1% chance of having another child who suffers from this
ailment.
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