What are the clinical symptoms of protein allergy in Canadian boys
4hw.org: many people will have all kinds of allergic reactions to different foods. Some people are allergic to wine, some people are allergic to fruit. But if they are allergic to protein, it's really difficult to maintain life, because the most important component of food is protein, and protein is also an important element to maintain life.
According to media reports, a boy in Canada recently suffered from a strange disease, which is known as food protein enterocolitis syndrome. He can only eat peaches to maintain his life.
Sometimes the world is also very cruel. There are always some strange diseases that endanger people's health and life. And these diseases are always after they appear. People begin to know them, and then try to overcome them. Therefore, they all pay a heavy price. Recently, a boy in Canada has a strange disease. At the age of 2, he can hardly eat any What can only survive by eating fresh organic peaches? It's because he has allergies when eating any food.
The boy named peros first fell ill when he was six months old. He began to have severe vomiting and diarrhea just after taking some complementary food. His parents couldn't figure out what was going on, so they had to take him to the hospital. But the doctors couldn't figure out what disease he had and didn't have any medicine to treat it. So they could only watch the children suffer Sin.
Later, it was diagnosed as food protein enterocolitis syndrome in an authoritative hospital. Later, in the course of physical examination, it was found that the boy also suffered from congenital thymus hypoplasia and 15q13.3 microdeletion syndrome. Whether these two diseases are necessarily related to food protein enterocolitis remains to be determined. However, it is now two-year-old children Zi can only live by eating fresh peaches. For him and his family, the burden is also very heavy.
His mother said that now it has been found that there is another liquid food formula to eat, but these foods are very expensive, and they can only be purchased with medical insurance next year, because their families can't afford such a high cost.
At present, the medical technology has not been able to treat the disease with specific drugs. However, the doctor said that the disease can gradually improve after the age of 3, but now the child is only two years old, and how to spend another year? For this reason, his mother began to seek some help from the society, hoping that someone could help them through the difficulties.
What is food protein enterocolitis syndrome? What kind of disease is it? What are the clinical symptoms? Let's get to know.
This is a disease that is allergic to milk, soybean and cereal, which means that children may have allergic reactions to all kinds of protein foods. Milk is animal protein and soybean is plant protein. These proteins have antagonistic effects and become allergic immediately after entering the body, and the main sites are small intestine and colon, which is mediated by a non IgE type immune response The main clinical symptoms are recurrent vomiting and severe diarrhea, which may lead to bloody stool.
The disease may last until the age of 3, and may improve later. However, there is no specific treatment drug in clinical practice, so we can only take some non allergic food to maintain life.
It seems that this kind of allergy is indeed more serious than the general food allergy. Unfortunately, there is no medicine to treat it. I can only hope that the little boy can successfully pass these difficult years between the ages of 2 and 3.