Alpha 1 antitrypsin deficiency is a genetic disorder that can cause multiple symptoms in the liver
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1. Liver disease
α1 antitrypsin is mainly synthesized in the liver, and its lack may lead to liver cell damage, which in turn leads to liver dysfunction. Common manifestations include fatigue, loss of appetite, etc. These symptoms may make people feel that the vitality of daily life is being weakened, like something wrong with the body's "engine".
2. Lung diseases
In cases of severe air pollution or long-term smoking
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3. Skin abnormalities
Due to the decrease in alpha1 antitrypsin levels, vascular endothelial function may be affected, resulting in increased capillary permeability. As a result, skin problems such as spider moles and lupus erythematosus may occur. These skin symptoms are like "signal lights" on the surface of the body, reminding us that there may be problems inside.
Patients may also experience other symptoms such as joint pain and hemolytic anemia. In order to avoid aggravation of the condition
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