Alpha 1 Antitrypsin
Test ID: A1AT A genetic disorder lack of Alpha-1 antitrypsin (AAT) deficiency is a common genetic disorder where a lack of AAT protein—produced in the liver—leads to premature emphysema (COPD) and liver disease. It is caused by inherited mutations (commonly the Z allele) causing dysfunctional or trapped AAT in the liver. Turnaround time: 1 day…
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