What is Hirschsprung's disease?
Hirschsprung's disease is a congenital condition that can cause extreme constipation, pain and fatal blockage of the intestine. Anemia, bloody stools and diarrhea can also be seen on the condition. Surgery, albeit intense, can treat the causes and most children with Hirschsprung's disease leads to normal lives after surgery. When the body cannot feel that the large intestine is full of waste products, the intestine can back up. In infants, this may be considered rarely of bowel movements that can be accompanied by painful convulsions. Due to larger bowel movements, sensitive skin around the rectum can tear and cause blood in the stool. Blood can also join in the large intestine.
Hirschsprung's disease is often difficult to diagnose in infants who are fed pattern. Sensitivity to ingredients in the formula often leads to constipation and painful stomachs. Often a few promises must be tested before we find the one that is easily digestible. The formula, although it uses many parents, cannot replicate ease of digestibleTheness associated with human breast milk.
Children with Hirschsprung's disease, which are exclusively breastfed, are likely to receive an earlier diagnosis, because theoretically nothing should disrupt the child's digestion and passage bowel movements during breast milk. In breastfed children, intestinal movements are usually quite soft and can occur several times a day. Pediatricians should be reported by lack of bowel movements, as this may also mean that it will not be successful or other intestinal disorders.
In some cases, even in breastfed children, the diagnosis of Hirschsprung's disease is delayed because breast milk can be affected by a mother who eats certain foods to which the child could be sensitive. In these cases, the presence of suspension in a child may first be released by removing food from the mother that could lead to allergies in an infant. Foods like milk, chocolate and coffee canbe suspicious.
When allergenic foods are removed and constipation is still present, pediatricians can administer a child to a pediatric gastroenterologist for further testing. The most common test methods used are the X -ray and Barya cell biopsy. Biopsy of cells, albeit more invasive, is a gold standard test, as the doctor may notice the absence of nerve cells and confirm Hirschsprung's disease.
Normal treatment for a person with Hirschsprung's disease is called a surgery. The non -functional part of the intestine is removed and the intestinal area with normal cells is connected again. This results in a healthy intestinal tract and has a high degree of success.
Sometimes children developed a significant infection in their large intestine surgery and must undergo an ostomy. In this procedure, the infected part of the intestine is first removed and the faecal matter is collected in the bag outside the body. This procedure is usually temporary and when the child regains health and strength, the pull passesEm.
children who did not have an early diagnosis of Hirschsprung's disease are exposed to a greater risk of life -threatening infections. They can also show poor growth and development and can vomit bile more often than healthy children. Symptoms of infection may include increased vomiting, diarrhea and high fever. If Hirschsprung's disease is suspected, such symptoms require immediate medical care.