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(Q41.9) Congenital absence, atresia and stenosis of small intestine, part unspecified
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54 128 in individuals diagnosis congenital absence, atresia and stenosis of small intestine, part unspecified confirmed
2 654 deaths with diagnosis congenital absence, atresia and stenosis of small intestine, part unspecified
5% mortality rate associated with the disease congenital absence, atresia and stenosis of small intestine, part unspecified
Diagnosis congenital absence, atresia and stenosis of small intestine, part unspecified is diagnosed Men are 9.30% more likely than Women
29 581
Men receive the diagnosis congenital absence, atresia and stenosis of small intestine, part unspecified
1 584 (5.4 %)Died from this diagnosis.
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Women receive the diagnosis congenital absence, atresia and stenosis of small intestine, part unspecified
1 070 (4.4 %)Died from this diagnosis.
Risk Group for the Disease congenital absence, atresia and stenosis of small intestine, part unspecified - 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, part unspecified
Absence or low individual and public risk
Congenital absence, atresia and stenosis of small intestine, part unspecified - what does this mean
Congenital absence, atresia and stenosis of the small intestine is a rare condition in which the small intestine is either missing, partially blocked, or abnormally narrow. this condition is usually present at birth and can cause severe malabsorption of nutrients, leading to poor growth and development.
What happens during the disease - congenital absence, atresia and stenosis of small intestine, part unspecified
Congenital absence, atresia and stenosis of the small intestine, part unspecified, is a birth defect caused by the improper development of the small intestine, resulting in a narrowing or blockage of the intestinal lumen and a decrease in the amount of nutrients and water that can be absorbed. this can be caused by a number of factors, including genetic mutations, environmental exposures, or a combination of both. in some cases, the cause may never be identified. the condition can lead to serious complications such as malnutrition, dehydration, and electrolyte imbalances. treatment usually involves surgical intervention to correct the defect and restore normal intestinal function.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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33 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital absence, atresia and stenosis of small intestine, part unspecified - Prevention
The best way to prevent congenital absence, atresia and stenosis of the small intestine is to ensure that pregnant women receive adequate pre-natal care, including regular check-ups and tests. additionally, it is important to ensure that pregnant women receive the appropriate nutrition and avoid any substances that could be harmful to the fetus.