How to treat Gaucher's disease?

Update Date: 2022-05-09 Source: Network

summary

Last month, one day, when I looked in the mirror, I suddenly found that my skin became very yellow. When I was sleeping or in daily activities, I felt a little bit difficult to breathe. Sometimes, even when I arrived at a restaurant, I had no appetite, as if I had a foreign body in my throat and could not swallow. Only after consulting the hospital did I know that I was suffering from Gaucher's disease. Let's take a look at the following.

How to treat Gaucher's disease?

The first is the manifestation of Gaucher's disease and the residual disease in the body β- The less the enzyme activity, the faster the symptoms. If the enzyme activity almost completely disappeared, then the condition deteriorated rapidly and brain symptoms appeared, then it showed infant type. If the enzyme activity was more, it showed juvenile type or adult type

Second: now we can use glucosidase extracted from the spleen of cattle for treatment, but also can use bone marrow transplantation and fibroblast transplantation for treatment, which has certain curative effect. In addition, some people also use kidney transplantation and spleen transplantation for treatment, which needs further study

Third: the disease is mainly symptomatic treatment, so we should strive for prenatal diagnosis, amniotic fluid cell culture in the mother's pregnancy, with extract determination β- If the glucosidase activity is almost completely disappeared, the possibility of infantile Gaucher's disease is high, the condition is serious, and the mortality is high

matters needing attention

When cervical spondylosis involves sympathetic nerve, dizziness, headache, blurred vision, distension and dryness of two eyes, tension of two eyes, tinnitus, ear blockage, imbalance, tachycardia, palpitation and chest tightness may occur.