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(Q41) Congenital absence, atresia and stenosis of small intestine
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54 128 in individuals diagnosis congenital absence, atresia and stenosis of small intestine confirmed
2 654 deaths with diagnosis congenital absence, atresia and stenosis of small intestine
5% mortality rate associated with the disease congenital absence, atresia and stenosis of small intestine
Diagnosis congenital absence, atresia and stenosis of small intestine is diagnosed Men are 9.30% more likely than Women
29 581
Men receive the diagnosis congenital absence, atresia and stenosis of small intestine
1 584 (5.4 %)Died from this diagnosis.
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Women receive the diagnosis congenital absence, atresia and stenosis of small intestine
1 070 (4.4 %)Died from this diagnosis.
Risk Group for the Disease congenital absence, atresia and stenosis of small intestine - 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 small intestine
Absence or low individual and public risk
Congenital absence, atresia and stenosis of small intestine - what does this mean
Congenital absence, atresia and stenosis of the small intestine is a birth defect where the small intestine is not fully formed, is blocked, or is too narrow. this can cause food to be unable to pass through the intestine, leading to poor nutrient absorption and malnutrition. it can also lead to an increased risk of infection due to the buildup of bacteria in the intestine.
What happens during the disease - congenital absence, atresia and stenosis of small intestine
Congenital absence, atresia and stenosis of the small intestine is a congenital disorder caused by a malformation of the small intestine during embryonic development. this malformation can lead to a narrowing or blockage of the small intestine, which can cause severe digestive problems, malabsorption, and malnutrition. this condition is usually diagnosed during infancy, and may require surgical intervention to correct the malformation and restore normal digestive functioning.
Clinical Pattern
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How does a doctor diagnose
- Physical examination to check for any abnormalities in the abdomen
- Laboratory tests to check for electrolyte imbalances
- X-ray or CT scan to check for any blockages in the intestine
- Ultrasound to check for any structural abnormalities in the intestine
- Endoscopy to check for any blockages in the intestine
- Colonoscopy to check for any blockages in the intestine
- Biopsy to check for any structural abnormalities in the intestine
Treatment and Medical Assistance
Main goal of the treatment: To improve the patient's ability to digest and absorb nutrients.
- Surgical intervention to correct structural abnormalities in the intestine
- Medication to reduce inflammation and pain
- Nutritional support to ensure adequate nutrition
- Ongoing monitoring of the patient's condition
- Counseling and support to help the patient cope with the condition
33 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital absence, atresia and stenosis of small intestine - Prevention
The best way to prevent congenital absence, atresia and stenosis of the small intestine is to ensure that pregnant women receive adequate prenatal care, including regular ultrasounds and tests to check for any abnormalities in the development of the fetus. additionally, it is important to ensure that women are getting the proper nutrition and avoiding any potential environmental risk factors that could lead to the development of this condition.