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(Q41.0) Congenital absence, atresia and stenosis of duodenum
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54 128 in individuals diagnosis congenital absence, atresia and stenosis of duodenum confirmed
2 654 deaths with diagnosis congenital absence, atresia and stenosis of duodenum
5% mortality rate associated with the disease congenital absence, atresia and stenosis of duodenum
Diagnosis congenital absence, atresia and stenosis of duodenum is diagnosed Men are 9.30% more likely than Women
29 581
Men receive the diagnosis congenital absence, atresia and stenosis of duodenum
1 584 (5.4 %)Died from this diagnosis.
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Women receive the diagnosis congenital absence, atresia and stenosis of duodenum
1 070 (4.4 %)Died from this diagnosis.
Risk Group for the Disease congenital absence, atresia and stenosis of duodenum - 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 duodenum
Absence or low individual and public risk
Congenital absence, atresia and stenosis of duodenum - what does this mean
Congenital absence, atresia and stenosis of duodenum is a rare congenital disorder in which the duodenum, the first part of the small intestine, is abnormally short, narrow, or absent. this condition is caused by a malformation of the duodenal tissue during fetal development. symptoms include vomiting, abdominal pain, and dehydration. treatment typically consists of surgical repair of the duodenum.
What happens during the disease - congenital absence, atresia and stenosis of duodenum
Congenital absence, atresia and stenosis of the duodenum is a condition in which the duodenum, the first part of the small intestine, is either absent, atretic or stenosed. this is caused by a failure of the duodenum to form properly during fetal development, leading to a narrowing or complete blockage of the lumen. this can lead to a variety of symptoms including malabsorption, abdominal pain, vomiting, and weight loss, as well as an increased risk of infection.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Abdominal ultrasound
- Abdominal CT scan
- Upper GI series
- Upper endoscopy
- Duodenal manometry
- Duodenal biopsy
- Barium swallow test
Treatment and Medical Assistance
Main goal of the treatment: To correct the congenital absence, atresia and stenosis of duodenum.
- Administer medication to reduce inflammation and pain.
- Perform X-rays and other imaging tests to diagnose the condition.
- Perform endoscopy to examine the duodenum.
- Perform surgical procedures to correct the abnormalities.
- Prescribe nutritional supplements to compensate for malabsorption.
- Monitor the patient's progress and adjust treatment as needed.
33 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital absence, atresia and stenosis of duodenum - Prevention
The best way to prevent congenital absence, atresia and stenosis of duodenum is to ensure that pregnant women receive adequate prenatal care, including regular ultrasounds and genetic testing. additionally, mothers should follow a healthy and balanced diet, take prenatal vitamins, and avoid smoking and alcohol during pregnancy.