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(Q42) Congenital absence, atresia and stenosis of large intestine
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132 235 in individuals diagnosis congenital absence, atresia and stenosis of large intestine confirmed
1 964 deaths with diagnosis congenital absence, atresia and stenosis of large intestine
2% mortality rate associated with the disease congenital absence, atresia and stenosis of large intestine
Diagnosis congenital absence, atresia and stenosis of large intestine is diagnosed Men are 18.58% more likely than Women
78 405
Men receive the diagnosis congenital absence, atresia and stenosis of large intestine
892 (1.1 %)Died from this diagnosis.
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53 830
Women receive the diagnosis congenital absence, atresia and stenosis of large intestine
1 072 (2.0 %)Died from this diagnosis.
Risk Group for the Disease congenital absence, atresia and stenosis of large intestine - Men and Women aged 0
In Men diagnosis is most often set at age 0-24, 30-34, 45-49, 65-69
Less common in men the disease occurs at Age 25-29, 35-44, 50-64, 70-95+Less common in women the disease occurs at Age 20-29, 35-69, 75-95+
In Women diagnosis is most often set at age 0-19, 30-34, 70-74
Disease Features congenital absence, atresia and stenosis of large intestine
Absence or low individual and public risk
Congenital absence, atresia and stenosis of large intestine - what does this mean
Congenital absence, atresia and stenosis of the large intestine is a rare congenital disorder in which the large intestine is either missing, abnormally narrow or blocked, preventing the normal passage of food and waste. this disorder is usually caused by a developmental abnormality of the gastrointestinal tract during fetal development.
What happens during the disease - congenital absence, atresia and stenosis of large intestine
Congenital absence, atresia and stenosis of large intestine is a condition caused by abnormal development of the large intestine during fetal development. this can be due to genetic mutations, environmental factors, or a combination of the two. it results in the failure of the large intestine to form correctly, leading to a narrowing of the lumen, malformations of the intestine, and the complete absence of sections of the intestine. this can lead to difficulty in nutrient absorption, malabsorption, and a variety of other complications.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- X-ray imaging
- Ultrasound imaging
- CT scan
- Barium enema
- Colonoscopy
- Blood tests
Treatment and Medical Assistance
Main Goal: To treat Congenital absence, atresia and stenosis of large intestine
- Perform surgery to correct the defect
- Administer antibiotics to prevent infection
- Prescribe medications to reduce inflammation and pain
- Administer nutrition through an IV or feeding tube
- Provide dietary guidance to ensure proper nutrition
- Monitor the patient’s progress and adjust treatment as needed
15 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital absence, atresia and stenosis of large intestine - Prevention
The best way to prevent congenital absence, atresia and stenosis of the large intestine is to ensure proper pre-natal care, including regular check-ups and adequate nutrition. additionally, genetic counseling and testing can help identify any potential risk factors for the development of these conditions.