How to treat genetic metabolic disease?

summary

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. If there are people suffering from this disease, we should pay attention to it. During the internship, I saw some common knowledge about the disease in a medical book. I have some knowledge about this disease, and I'd like to share it with you.

How to treat genetic metabolic disease?

First: people who have studied biology know that people are inherited through genes in chromosomes. Some people think that they 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, it can have a selective abortion, 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: for pre symptomatic treatment, now because the neonatal screening of hereditary metabolic diseases is widely carried out, the disease can be diagnosed before the symptoms appear, which opens up a good prospect for pre symptomatic 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.