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(Q41.2) Congenital absence, atresia and stenosis of ileum
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54 128 in individuals diagnosis congenital absence, atresia and stenosis of ileum confirmed
2 654 deaths with diagnosis congenital absence, atresia and stenosis of ileum
5% mortality rate associated with the disease congenital absence, atresia and stenosis of ileum
Diagnosis congenital absence, atresia and stenosis of ileum is diagnosed Men are 9.30% more likely than Women
29 581
Men receive the diagnosis congenital absence, atresia and stenosis of ileum
1 584 (5.4 %)Died from this diagnosis.
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Women receive the diagnosis congenital absence, atresia and stenosis of ileum
1 070 (4.4 %)Died from this diagnosis.
Risk Group for the Disease congenital absence, atresia and stenosis of ileum - Men and Women aged 0
In Men diagnosis is most often set at age 0-24, 60-64
Less common in men the disease occurs at Age 25-59, 65-95+Less common in women the disease occurs at Age 10-14, 25-29, 45-95+
In Women diagnosis is most often set at age 0-9, 15-24, 30-44
Disease Features congenital absence, atresia and stenosis of ileum
Absence or low individual and public risk
Congenital absence, atresia and stenosis of ileum - what does this mean
Congenital absence, atresia, and stenosis of the ileum is a rare condition where the ileum, a portion of the small intestine, is either missing, abnormally narrow, or blocked. this condition is usually present at birth, and is caused by abnormal development of the ileum during fetal development.
What happens during the disease - congenital absence, atresia and stenosis of ileum
Congenital absence, atresia and stenosis of ileum is a rare congenital malformation of the small intestine, which is caused by an abnormal development of the embryonic tissue during the first trimester of pregnancy. this malformation can lead to a decreased absorption of nutrients, as well as an impaired motility of the small intestine, resulting in malabsorption and malnutrition. additionally, it can lead to an accumulation of fluid in the abdomen, as well as an increased risk of infection.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete physical examination
- Abdominal X-ray
- Abdominal ultrasound
- Barium enema
- CT scan
- Colonoscopy
- Endoscopy
- Small bowel follow-through
- Laparoscopy
Treatment and Medical Assistance
Main goal of the treatment: To restore or improve the digestive system's functioning.
- Surgery to correct the atresia or stenosis
- Gastrointestinal reconstruction to restore the digestive system's functioning
- Nutritional support
- Antibiotic therapy to prevent infections
- Regular monitoring of the patient's condition
- Regular follow-up with a gastroenterologist
- Regular blood tests to monitor the patient's health
33 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital absence, atresia and stenosis of ileum - Prevention
The best way to prevent congenital absence, atresia and stenosis of ileum is to ensure that pregnant women receive proper prenatal care and nutrition, as well as avoiding exposure to environmental toxins. additionally, genetic counseling and testing may be beneficial for those with a family history of this condition.