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What tests does the baby's silkworm disease need to do?
Silkworm bean disease is a genetic disease. The first thing to do is blood test, mainly to see the activity of glucose hexaphosphatase. If the value is normal or high, there is no problem. But if the activity is low, it may be silkworm disease.

This is an invisible genetic disease caused by congenital glucose hexaphosphatase deficiency. This disease usually requires lifelong companionship, but it makes little difference to normal people, except that some drugs or foods cannot be eaten.

Generally speaking, mothers with silkworm disease genes will not suffer from this disease. If the mother has a younger brother or elder brother, the disease will happen. Self-healing is possible, especially for premature babies G6pd enzyme may be low at birth, and may be normal after growing up. However, this test is not performed in general pregnancy tests.

If the patient eats broad beans by mistake, the patient will have acute intravascular hemolysis within 1-2 days. Once the disease breaks out, it will break out violently, showing general malaise, pallor, mild fever, dizziness, fatigue, loss of appetite, abdominal pain, nausea and deepening urine color. Jaundice, anemia, hemoglobinuria, and urine are soy sauce-colored, and then the body temperature rises, and fatigue and fatigue intensify for about 3 days.

When it occurs at the same time as hemolytic anemia, it will aggravate vomiting, diarrhea and abdominal pain, and appear hepatomegaly and abnormal liver function. About 50% patients have large spleen. Severe cases may lead to coma, shock and general failure. If the first aid is not as good as usual,1-will die within 2 days.

But although the situation is not good, as long as you pay attention to your diet every day. Don't eat broad beans and their products, but pay special attention to some bean products, so it won't be too dangerous.