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(Q41.1) Congenital absence, atresia and stenosis of jejunum
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54 128 in individuals diagnosis congenital absence, atresia and stenosis of jejunum confirmed
2 654 deaths with diagnosis congenital absence, atresia and stenosis of jejunum
5% mortality rate associated with the disease congenital absence, atresia and stenosis of jejunum
Diagnosis congenital absence, atresia and stenosis of jejunum is diagnosed Men are 9.30% more likely than Women
29 581
Men receive the diagnosis congenital absence, atresia and stenosis of jejunum
1 584 (5.4 %)Died from this diagnosis.
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24 547
Women receive the diagnosis congenital absence, atresia and stenosis of jejunum
1 070 (4.4 %)Died from this diagnosis.
Risk Group for the Disease congenital absence, atresia and stenosis of jejunum - 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 jejunum
Absence or low individual and public risk
Congenital absence, atresia and stenosis of jejunum - what does this mean
Congenital absence, atresia and stenosis of jejunum is a rare condition in which the jejunum, a part of the small intestine, is either completely absent, narrowed, or blocked. this condition is usually caused by abnormal development in the womb, and can cause digestion and absorption problems, as well as vomiting and abdominal pain.
What happens during the disease - congenital absence, atresia and stenosis of jejunum
Congenital absence, atresia and stenosis of jejunum is a condition in which the jejunum, the middle section of the small intestine, is missing or narrowed. this condition can be caused by a variety of factors, including genetic mutations, environmental exposures, and other medical conditions. it can lead to malabsorption, malnutrition, and gastrointestinal symptoms such as abdominal pain, bloating, and diarrhea. in some cases, surgical interventions may be necessary to correct the problem.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Laboratory tests (blood, urine, stool)
- Imaging tests (ultrasound, CT scan, MRI)
- Endoscopy
- Genetic testing
- Biopsy
Treatment and Medical Assistance
Main goal: To treat the congenital absence, atresia and stenosis of jejunum.
- Prescribe medications to reduce inflammation and pain
- Administer antibiotics to prevent infection
- Perform endoscopy to diagnose the condition
- Perform surgery to remove any blockages
- Perform reconstructive surgery to restore jejunal function
- Provide nutritional support to maintain normal growth and development
- Monitor 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 jejunum - Prevention
The best way to prevent congenital absence, atresia and stenosis of jejunum is to ensure good antenatal care during pregnancy. this includes regular check-ups with an obstetrician, eating a healthy diet, avoiding alcohol and smoking, and taking prenatal vitamins. additionally, genetic counseling should be sought if there is a family history of the condition.