Imperforate anus: Difference between revisions
CSV import Tags: mobile edit mobile web edit |
CSV import |
||
| Line 33: | Line 33: | ||
{{stub}} | {{stub}} | ||
<gallery> | |||
File:Atresia.jpg|Imperforate anus | |||
</gallery> | |||
Revision as of 00:40, 20 February 2025
Imperforate anus is a birth defect that affects about one in every 5,000 newborns, in which the rectum is malformed. The rectum is the end of the digestive system, where stool exits the body. In babies with imperforate anus, the rectum does not connect to the anus.
Causes
The exact cause of imperforate anus is unknown. It is thought to occur early in fetal development. Some studies suggest that it may be related to genetic factors, but more research is needed to confirm this.
Symptoms
The main symptom of imperforate anus is the absence of a normal rectal opening. Other symptoms can include:
- Abdominal swelling
- Failure to pass stool within the first 48 hours of life
- Unusual stooling patterns, such as passing stool from the urethra in boys or the vagina in girls
Diagnosis
Imperforate anus is usually diagnosed shortly after birth during a physical examination. Additional tests may be needed to determine the severity of the condition and to check for associated anomalies. These can include:
Treatment
Treatment for imperforate anus usually involves surgery to create a new rectal opening. The type of surgery depends on the severity of the condition and the presence of associated anomalies. Some children may need additional surgeries or treatments as they grow.
Prognosis
With early diagnosis and treatment, most children with imperforate anus can lead normal lives. However, they may have ongoing issues with bowel control and may need long-term follow-up care.
