What symptom does infant metabolize disease have

summary

Hereditary metabolic disease, as the name suggests, is a hereditary disease. Now let's give a brief introduction to the symptoms of hereditary metabolic diseases, such as deafness, visual impairment, vomiting, and mental retardation. During the internship in the hospital, I happened to read hereditary metabolic disease in a medical book, and I had some understanding of this disease. Now I would like to share with you some common sense things about hereditary metabolic diseases, hoping to help you.

What symptom does infant metabolize disease have

First: people who have studied biology know that according to the doctor's advice, people are inherited through the genes in the chromosome. Some people don't want to read it because they can't understand it. It's not as hard as you think. Genetic metabolic disease is a kind of genetic disease with defective metabolic function, and there are also causes of genetic diseases. It is usually manifested as mental retardation, anemia, vomiting, diarrhea, etc.

Second: if a child is found to have a genetic metabolic disease before birth, and know more about the symptoms of some related diseases, then selective abortion can be carried out, and the baby does not want to be sick at birth. Or choose medication and diet. The baby's physical development will have a certain impact.

Third: 3 for pre symptom treatment, it is good for the health to ensure a normal diet. Now, due to the extensive neonatal screening of hereditary metabolic diseases, the disease can be diagnosed before the symptoms appear, which opens up a good prospect for pre symptom treatment. In the early stage of drug treatment, such as penicillamine or dimercaptopropanol treatment, can achieve the purpose of disease free. There is also diet therapy, that is, targeted selection of substances contained in milk powder and other products.

matters needing attention

For patients who are suffering from symptoms, they should control the consumption of some foods. At the same time, drug treatment should be carried out. Some inherited metabolic diseases are caused by genetic inheritance. Some of the acquired mutations cause the incidence rate of the newborn, which covers not only the whole age. Therefore, we should pay attention to whether we have this disease