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Alpha-1 Antitrypsin Deficiency

A genetic disease with significant underdiagnosis.

Alpha‑1 Antitrypsin Deficiency is a common inherited disorder characterized by a quantitative and/or qualitative deficiency of the protease inhibitor α1‑antitrypsin (AAT). Individuals with AAT deficiency are at increased risk of developing chronic obstructive pulmonary disease (COPD) and chronic liver disease.

Alpha‑1 Antitrypsin Deficiency (AATD) is a rare hereditary disorder characterized by reduced levels of alpha‑1 antitrypsin, which can lead to serious lung and liver disease in both children and adults.

Knowledge & Science

Instruments for diagnosing Alpha-1 Antitrypsin Deficiency

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Carefully read the instructions in the reagent package inserts and instrument manuals.