Call : +91 97756 00057
Intestinal atresia is a congenital condition and can be described as a broad spectrum of birth defects that end in a blockage in either the tiny or intestine. During normal fetal development, the intestines remain unobstructed, allowing contents from the stomach to flow freely through the baby’s alimentary canal. When a blockage (atresia) occurs, however, the intestines lose some or all of their ability to soak up nutrients and to push food and fluids through the baby’s alimentary canal. Consult with the paediatric surgeon for the best intestinal atresia treatment in Siliguri.
Duodenal atresia involves a blockage of the upper part of the tiny intestine or duodenum. It results from a special disease process than other sorts of intestinal atresia and is usually related to additional birth defects. Consult with the paediatric surgeon for the best intestinal atresia treatment in Siliguri.
The various kinds of intestinal atresia are:
Intestinal atresia may be a congenital condition, which suggests it develops before birth. The malformation is assumed to be a “vascular accident” that happens when the blood supply to the unborn babies intestines is unexpectedly interrupted. the rationale for the reduction within the blood supply is unknown. In most cases, it probably occurs sporadically (for no identifiable reason), but some research suggests that certain medications taken during pregnancy may raise the danger. Genetic factors can also play a task.
Your baby will need specialized medical aid after birth and can therefore be taken to our NICU. Most babies with intestinal atresia are comfortable breathing on their own. Treatment for intestinal atresia requires an operation to get rid of the blockage (atresia) and repair the affected part of the intestine. The surgery isn't considered an emergency and is usually done when the baby is 2 or three days old.Consult with the paediatric surgeon for the best intestinal atresia treatment in Siliguri.