Alpha-1 Antitrypsin Deficiency
Alpha-1 antitrypsin deficiency is a genetic disorder that can cause lung disease (like emphysema) and liver disease. It results from low levels of alpha-1 antitrypsin, a protein that protects the lungs from inflammation.
Common Symptoms
- Shortness of breath
- Wheezing
- Fatigue
- Jaundice (in infants)
- Swelling of legs and abdomen (adults with liver disease)
Clinical Sources
- Alpha-1 Antitrypsin Deficiency: Causes, Symptoms & TreatmentCleveland Clinic
Diagnostic Lab Tests
Tests commonly used to diagnose or monitor Alpha-1 Antitrypsin Deficiency:
Alpha-1 Globulin
Fraction of serum protein....
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Karyotyping Analysis
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TCF3-HLF Translocation [t(17;19)]
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Hepatitis B Surface Antigen (HBsAg)
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H.C.V. ELISA
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Alpha-1 Globulin
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Anti HAV Antibodies
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Liver-Kidney Microsome (LKM)-1 Antibody (ELISA)
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